FCC ID: Z7A-SDMACP Embedded Wireless module

PPrrooCCuuiittyy BBeedd SSeerriieess OOppeerraattiioonnss MMaannuuaall 3009 3009-009-001 Rev A.0 2020/05 EN SSyymmbboollss Refer to instruction manual/booklet Consult instructions for use General warning Caution Warning; electricity Fuse rating Non-ionizing radiation Catalogue number Serial number European medical device CE mark Manufacturer Safe working load Mass of equipment NAWI Class IIII Maximum patient weight Authorized representative in the European Community For US Patents see www.stryker.com/patents 3009-009-001 Rev A.0 EN Adult patient Alternating current Direct current Duty cycle of product Protective earth ground IIPPXX44 Protection from liquid splash Type B applied part Unit provides terminal for connection of a potential equalization conductor. The potential equalization conductor provides direct connection between the unit and potential equalization busbar of the electrical installation. Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012 C1:2009/(R)2012 and A2:2010/(R)2012, CAN/CSA-C22.2 No. 60601-1:14, IEC 60601-2-52:2009/A1:2015, CAN/CSA-C22.2 No. 60601-2-52:11 with Amendment 1:2017. In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic Equipment (WEEE) as amended, this symbol indicates that the product should be collected separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor for disposal information. Ensure infected equipment is decontaminated prior to recycling. EN 3009-009-001 Rev A.0

~ 2m 18m87VL TTaabbllee ooff CCoonntteennttss Warning/Caution/Note Definition ..............................................................................................................................3 Summary of safety precautions ................................................................................................................................3 Introduction ...............................................................................................................................................................6 Product description .................................................................................................................................................6 Indications for use...................................................................................................................................................6 Expected service life ...............................................................................................................................................7 Disposal/recycle.................................................................................................................................................7 Contraindications ....................................................................................................................................................7 Specifications .........................................................................................................................................................7 Wi-Fi radio specifications (option) ........................................................................................................................9 Bluetooth radio specifications (option)................................................................................................................10 System requirements and recommendations for iiBBeedd Wireless (option) ....................................................................10 iiBBeedd Wireless data usage (option) .....................................................................................................................10 Customer network communication requirements for iiBBeedd Wireless (option) ..........................................................11 Product illustration ................................................................................................................................................12 Applied parts ........................................................................................................................................................13 Contact information ...............................................................................................................................................13 Serial number location...........................................................................................................................................13 Setup.......................................................................................................................................................................14 Setting up iiBBeedd Wireless (option) ...........................................................................................................................14 Setting up wired nurse call communication..............................................................................................................14 Setting up wireless nurse call communication..........................................................................................................15 Operation ................................................................................................................................................................16 Plugging or unplugging the product ........................................................................................................................16 Charging the battery..............................................................................................................................................16 Storing the power cord ..........................................................................................................................................17 Transporting the product........................................................................................................................................17 Applying or releasing the brakes ............................................................................................................................18 Applying or releasing steer lock..............................................................................................................................18 Activating the CPR release handle .........................................................................................................................19 Removing or replacing the headboard ....................................................................................................................19 Removing or replacing the footboard ......................................................................................................................20 Raising the siderails ..............................................................................................................................................20 Lowering the siderails............................................................................................................................................20 Securing a Foley bag to the Foley bag hook ............................................................................................................21 Activating nurse call ..............................................................................................................................................21 Connecting peripheral equipment to the auxiliary outlet............................................................................................21 Operator control panel, basic, outside siderail .........................................................................................................21 Operator control panel, advanced, outside siderail (option) ......................................................................................22 Patient control panel, inside siderail........................................................................................................................23 Pendant, basic (option)..........................................................................................................................................24 Pendant, advanced (option) ...................................................................................................................................24 Footboard control panel - Menu controls .................................................................................................................24 Footboard control panel - Position ..........................................................................................................................25 Footboard control panel - Motion Lock ....................................................................................................................26 Footboard control panel - Scale..............................................................................................................................26 Zeroing/taring the scale ....................................................................................................................................27 Weighing a patient............................................................................................................................................28 Adding or removing equipment ..........................................................................................................................28 Footboard control panel - Bed exit ..........................................................................................................................29 Arming or disarming bed exit .............................................................................................................................29 Footboard control panel - iiBBeedd Watch ....................................................................................................................30 Enabling or disabling iiBBeedd Watch ......................................................................................................................31 Footboard control panel - Settings..........................................................................................................................31 Accessories and parts ............................................................................................................................................33 3009-009-001 Rev A.0 1 EN Raising or lowering the IV pole (option)...................................................................................................................33 Attaching or removing the patient helper (option) .....................................................................................................34 Adjusting the patient helper (option) .......................................................................................................................35 Attaching the oxygen bottle holder..........................................................................................................................36 Cleaning and disinfecting with wipes......................................................................................................................37 Cleaning..................................................................................................................................................................38 Disinfecting .............................................................................................................................................................39 Preventive maintenance .........................................................................................................................................40 Wireless notifications ..............................................................................................................................................41 EMC information .....................................................................................................................................................42 EN 2 3009-009-001 Rev A.0 WWaarrnniinngg//CCaauuttiioonn//NNoottee DDeeffiinniittiioonn The words WWAARRNNIINNGG, CCAAUUTTIIOONN, and NNOOTTEE carry special meanings and should be carefully reviewed. Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe potential serious adverse reactions and safety hazards. WWAARRNNIINNGG CCAAUUTTIIOONN Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient or damage to the product or other property. This includes special care necessary for the safe and effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or misuse. NNoottee -- Provides special information to make maintenance easier or important instructions clearer. SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel. WWAARRNNIINNGG Always use Stryker approved support surfaces that have been tested for compatibility with the product frame to avoid the risk of patient entrapment. Always plug the product into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade wall outlet. This product is equipped with a hospital-grade plug for protection against electric shock hazard. Always map the iiBBeedd Locator or SSeeccuurree Connect Locator to the location to provide location information. If you move an iiBBeedd Locator or SSeeccuurree Connect Locator after it has been set up and mapped, you must remap to the new location. Always use a Stryker supplied interface cable. Use of any other cable may cause the product to not function as intended, which may result in patient or user injury. Always connect this product to a supply mains with protective earth to avoid the risk of electric shock. Always make sure the product is connected to an appropriate power source if the loss of power would result in Always allow enough clearance between the head end of the product and the adjacent wall, so you can unplug the unacceptable risk. power cord from the wall outlet. Always store the power cord before you transport the product. Always disconnect the power cord from the wall outlet if you detect overheating of the battery, cables, or cords. Do not use the product until it has been inspected, serviced, and confirmed to work as intended by maintenance personnel. Always replace the battery after it surpasses its expected service life. Do not open the battery. Do not expose the battery to excessive heat. Do not spill liquid onto the battery or submerge the battery in liquid. Always store the power cord to avoid the risk of entanglement, damage to the power cord, or potential shock hazards. If the power cord is damaged, remove the product from service. Always use two people when you transport the product. Always lock the siderails in the full up position with the sleep surface horizontal when you transport a patient. Always keep limbs, hands, fingers, and other body parts clear of mechanisms and gaps. Always make sure that there are no obstacles near the product. Injury to the patient, operator, bystanders or damage to the frame or surrounding equipment could occur if you collide with an obstacle. Do not attempt to transport the product laterally. This may cause the product to tip. Always apply the brakes when a patient is getting into or out of the product to avoid instability. Always apply the brakes when the patient is unattended. Do not apply the brakes to slow or stop the product while the product is in motion. 3009-009-001 Rev A.0 3 EN with steer lock. of the product. falls. product. Always unplug the power cord before you transport the product. Always release the brakes before you transport the product. Do not transport the product with the brakes applied. Do not transport the product laterally after you apply the steer lock pedal. The product cannot swivel when you transport Do not attempt to release steer lock while the product is in motion. Do not use the headboard for CPR support. Always set the siderail position for appropriate patient safety. Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts Only use hospital grade electric equipment consuming 5A or less with the auxiliary outlet. The use of standard electric equipment may bring the current leakage to a level unacceptable for hospital equipment. Do not use the auxiliary outlet for life sustaining equipment. Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient Always lock the controls when the patient's condition requires extra safety measures. Do not use the scale system reading as a reference for medical treatment. The scale system assists only to monitor the patients weight variation. Do not use bed exit to replace patient monitoring protocol, it is intended only to aid in the detection of a patient exiting the Always use two people to attach or remove the patient helper. Do not load the patient helper above the safe working load of 200 lb (90.7 kg). Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be no closer than 12 inches (30 cm) to any part of PPrrooCCuuiittyy bed series, including cables specified by the manufacturer. Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the product. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they operate properly. The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation. CCAAUUTTIIOONN Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. Do not clean, disinfect, service, or perform maintenance while the product is in use. Always plug the product into a hospital grade protective earthed outlet when not in use to maintain a sufficient battery charge and to maximize product performance while operating on battery power. Always replace batteries that have corrosion at the terminals, display cracking, have expanded or bulging sides, or no Always use authorized batteries when you replace the batteries. Use of unauthorized batteries may lead to longer can maintain a full charge. unpredictable system performance. Do not pinch the power cord in the bed frame. Do not use the siderails as a push or pull device. Always move the product using the integrated handles in the headboard and footboard. Always remove the patient helper before you transport the product. Do not use the patient helper as a push or pull device. Do not use the oxygen bottle holder as a push or pull device. Do not use the IV pole as a push or pull device. Always make sure that the IV pole is at a low height during transport. Always make sure that all persons and equipment are away from the area below and around the Fowler before you activate the CPR release handle. The CPR release handle is for emergency use only. Always make sure that the product is clear of obstacles before you use motion functions. Do not load the IV pole above the safe working load of 40 lb (18 kg). EN 4 3009-009-001 Rev A.0 Do not load an individual IV pole hook above the safe working load of 20 lb (9 kg). Always secure the lifting pole in the mounting bracket before you adjust the patient helper. Always make sure that the patient helper mounting bracket is secure before use. Do not load the oxygen bottle holder above the safe working load of TBD lb. Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors. Remove the occupant from the product, clean up the fluid, and inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product. Do not return the product to service until dry and tested for safe operation. Always wipe down with clean water (or 70% isopropyl alcohol, if using VViirreexx TB) and dry each product after disinfecting. Some disinfectants are corrosive in nature and may cause damage to the product. If you do not rinse and dry the product, you may leave a corrosive residue on the surface of the product. This corrosive residue could cause premature degradation of critical components. Failure to follow these disinfecting instructions may void your warranty. 3009-009-001 Rev A.0 5 EN IInnttrroodduuccttiioonn This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance of this product. CCAAUUTTIIOONN Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. NNoottee This manual is a permanent part of the product and should remain with the product even if the product is sold. Stryker continually seeks advancements in product design and quality. This manual contains the most current product information available at the time of printing. There may be minor discrepancies between your product and this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770. PPrroodduucctt ddeessccrriippttiioonn The Stryker Model 3009 PPrrooCCuuiittyy bed series is a powered, adjustable hospital bed with a patient support surface. The product contains siderails that you can lock into three positions, a headboard, and a footboard. The product has Fowler, Gatch, and lift articulation capabilities, which aid to adjust surface contour, angle, and bed height. The product transports patients aided by the optional ZZoooomm function. The product features manual and electronic brakes. Product height range is adjustable between 11.5 inches to 32 inches. The Fowler raises to 70 degrees. Various options are available, including iiBBeedd Watch, iiBBeedd Wireless, scale, bed exit, auxiliary AC outlet option, IV pole, and defibrillator tray. Integrated scale to track patient weight fluctuation throughout a patients stay. iiBBeedd Watch to set various bed parameters to track bed position. Both iiBBeedd Watch and the bed exit system provide visual and audible alerts. iiBBeedd Wireless to monitor product parameters that a healthcare provider (HCP) views or sets at the bedside or from a remote location. Motion and feature lockouts, set by the HCP, to limit patient accessible controls for compliance to set bed parameters. Nurse call capability through a wired connection or wireless headwall. IInnddiiccaattiioonnss ffoorr uussee The 3009 PPrrooCCuuiittyy bed series is intended for use to assist with positioning, therapy, recovery, support, and transport of patients within an acute care facility. The intended user is both HCPs (nurses, nurse aides, and medical doctors) and human patients. This product can be used with both adult and pediatric patients that weigh more than 60 lb, with a maximum height of 84 inches without bed extender or 96 inches with bed extender. The scale output is not intended to be used to determine diagnosis or treatment. iiBBeedd Wireless with iiBBeedd Watch provides clinical staff the ability to set, adjust, and monitor specific bed parameters from a remote location within a healthcare facility through bidirectional data communication. The bed parameters include bed brake status, siderail position, bed exit zone and sensitivity, iiBBeedd Watch enablement, bed motion lock, and bed scale observation. The desired bed parameters will be set by clinicians at bedside. iiBBeedd Wireless with iiBBeedd Watch is intended for use only with specific enabled Stryker beds that are verified and validated with the iiBBeedd Wireless software and is not intended to provide bed status information for non-Stryker beds. Patient health information is not communicated or stored. This product is not intended for use with:

EN 6 3009-009-001 Rev A.0 Behavioral health patient use Newborn (neonate) or infant patient use Oxygen rich environments Home care or long-term care facility settings EExxppeecctteedd sseerrvviiccee lliiffee DDiissppoossaall//rreeccyyccllee CCoonnttrraaiinnddiiccaattiioonnss None known. SSppeecciiffiiccaattiioonnss The PPrrooCCuuiittyy bed series has a 10 year expected service life under normal use conditions and with appropriate periodic maintenance. The backup batteries have a one year expected service life under normal use conditions. Always follow the current local recommendations and/or regulations governing environmental protection and the risks associated with recycling or disposing of the equipment at the end of its useful life. WWAARRNNIINNGG -- Always use Stryker approved support surfaces that have been tested for compatibility with the product frame to avoid the risk of patient entrapment. Safe working load NNoottee:: Safe working load indicates the sum of the occupant, accessories, and mattress weight. 550 lb 249.5 kg Maximum patient weight Mass of equipment with safe working load Standard ZZoooomm (ZM option) Standard ZZoooomm (ZM option) Product weight Scale system capacity maximum Scale system accuracy (non-NAWI) Scale system accuracy (NAWI) MAX = 250 kg, MIN = 20 kg, e = 2 kg, Tare = -60 kg 500 lb 1000 lb 1100 lb 450 lb 550 lb 551.2 lb 226.8 kg 453.6 kg 499 kg 204.1 kg 249.5 kg 250 kg 3 lb (1.4 kg) of the total patient weight for patients who weigh 60 lb (27.2 kg) to 100 lb (45.4 kg) 3% of the total patient weight for patients who weigh 100 lb (45.4 kg) to 550 lb (249.5 kg) 2.2 lb (1 kg) for patients who weigh 44 lb (20 kg) to 220 lb (100 kg) 4.4 lb (2 kg) for patients who weigh 220 lb (100 kg) to 551 lb (250 kg) Patient sleep surface Standard 84 in. x 35 in. 213.4 cm x 88.9 cm 3009-009-001 Rev A.0 7 EN Bed height to top of seat litter Gatch position Fowler position Trendelenburg and reverse Trendelenburg Electrical requirements With bed extender accessory 94.5 in. x 35 in. 240 cm x 88.9 cm Standard Zoom 12 in. to 30 in. 30.5 cm x 76.2 cm 14 in. to 32 in. 35.6 cm x 81.3 cm 0 to 30 5 0 to 65 5

+12 to -12 5 NNoottee -- Class I Electrical Equipment: Protection against electrical shock relies on connection to protective earth of an appropriately rated hospital grade outlet. 120 VAC, 60 Hz, 8A 230 VAC, 50 Hz, 4A Hospital grade auxiliary outlet 120 VAC, 60 Hz, 8A 230 VAC, 50 Hz, 4A NNoottee -- Always replace with Stryker approved batteries. 12 VDC, 1.2 Ah (x2) (Stryker part number:

700000341245) 2 minutes ON, 18 minutes OFF 1, 2, 3, and 5 per IEC 60601-2-52 Maximum acoustic sound pressure 64 dBa LLeennggtthh WWiiddtthh TThhiicckknneessss 84.25 in. 214 cm 35.5 in. 90.2 cm 9.5 in. 24.1 cm 213.4 cm 35 in. 88.9 cm 213.4 cm 35 in. 88.9 cm 213.4 cm 35 in. 88.9 cm 213.4 cm 35 in. 88.9 cm 7 in. 6 in. 6 in. 7 in. 17.8 cm 15.2 cm 15.2 cm 17.8 cm 84 in. 213.4 cm 35 in. 88.9 cm 8-10.5 in. 20.3-26.7 cm Battery voltage Duty cycle Application environments CCoommppaattiibbllee ssuuppppoorrtt ssuurrffaacceess Model 2850 CCoommffoorrttGGeell Model 2860 IIssooFFlleexx Model 2872 IIssooTToouurr Model 2815 PPrrooFFoorrmm Model 2940 IIssooAAiirr Model 2973 IIssoolliibbrriiuumm

(ZM option only) 84 in. 84 in. 84 in. 84 in. Stryker reserves the right to change specifications without notice. Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations. EN 8 3009-009-001 Rev A.0 EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn Ambient temperature Relative humidity (non-condensing) WWii--FFii rraaddiioo ssppeecciiffiiccaattiioonnss ((ooppttiioonn)) Atmospheric pressure Manufacturer/model Chipset IEEE 802.11 RF bands Encryption Authentication 802.1X Client certificates Supported data rates Hash function compatibility Channel plan Other IItteemm Operating frequencies Silex SX-SDMAC-2832S+

Qualcomm QCA9377-3 a/b/g/n/ac 2.4 GHz, 5 GHz AES and TKIP

(TKIP is not supported with WPA2) WPA Personal/Enterprise and WPA2 Personal/Enterprise PEAP-MSCHAP - v2 Stryker iiBBeedd Wireless client(s) cannot accept or upload certificates 802.11b/g: 1-54 Mbps 802.11a: 6-54 Mbps 802.11n: MCS0-7 802.11ac: MCS0-9 (compatible) SHA-1 and SHA-2 server side certificate recognition for PEAP-MSCHAP - v2 2.4 GHz: All Channels Supported 5 GHz: All Channels Supported

(Recommend against the use of DFS and ISM Channels) Leverage hospital SSID Support for 802.11r Support for Cisco CCX (Fast roaming) SSppeecciiffiiccaattiioonn -- CChhiippsseett QQCCAA99337777--33 ((QQuuaallccoommmm AAtthheerrooss)) BBaanndd 2.4GHz MMooddee 11b 11g/n/ac MMiinn 2412 2412 MMaaxx 2472 2472 UUnniitt MHz MHz 3009-009-001 Rev A.0 9 EN 95 F(35 C)50 F(10 C) 140 F(60 C)-40 F(-40 C)75%30%95%10%106 kPa70 kPa106 kPa50 kPa IItteemm SSppeecciiffiiccaattiioonn -- CChhiippsseett QQCCAA99337777--33 ((QQuuaallccoommmm AAtthheerrooss)) BBaanndd 5GHz 2.4GHz 5GHz MMooddee 11g/n/ac 11a/n/ac 11n/ac 11ac 11b/g/n 11a/n/ac 11n/ac 11ac 11b MMiinn 2422 5180 5190 5210 MMaaxx 2462 5825 5795 5775 5 20 40 80 Frequency steps Not applicable DSSS (DBPSK, DQPSK, CCK) Not applicable Modulation types Not applicable 11a/g/n Not applicable 11ac OFDM (BPSK, QPSK, 16QAM, 64QAM) OFDM (BPSK, QPSK, 16QAM, 64QAM, 255QAM) Not applicable Not applicable Maximum ERP Not applicable Not applicable

-8.648 dBW BBlluueettooootthh rraaddiioo ssppeecciiffiiccaattiioonnss ((ooppttiioonn)) IItteemm Operating frequencies SSppeecciiffiiccaattiioonn -- CChhiippsseett WWTT3322ii ((SSiilliiccoonn LLaabbss)) CChhaannnneell 79 MMiinn 2.4 MMaaxx 2.4835 Receiving bandwidth Not applicable Maximum ERP Not applicable 1

-21.148 UUnniitt MHz MHz MHz MHz MHz MHz MHz MHz UUnniitt GHz MHz dBW SSyysstteemm rreeqquuiirreemmeennttss aanndd rreeccoommmmeennddaattiioonnss ffoorr iiBBeedd WWiirreelleessss ((ooppttiioonn)) To implement iiBBeedd Wireless, follow these requirements for hardware, software, and communication, product specifications, required settings, and recommendations. NNoottee -- If minimum system requirements are not met, system performance will be impacted. iiBBeedd WWiirreelleessss ddaattaa uussaaggee ((ooppttiioonn)) iiBBeedd Wireless uses 10-15 KB per connected Wi-Fi radio every 40 seconds. iiBBeedd Wireless uses an additional 15-40 KB per Wi-Fi radio for each subscription created by a third-party vendor like Connexall, Capsule, Epic, and Cerner. NNoottee -- Based on network conditions, Wi-Fi radio messages are typically sent within five minutes when connected. This depends on product activity like when you apply the brakes, adjust the rails, alarms, and how the third-party defines subscription times. EN 10 3009-009-001 Rev A.0 CCuussttoommeerr nneettwwoorrkk ccoommmmuunniiccaattiioonn rreeqquuiirreemmeennttss ffoorr iiBBeedd WWiirreelleessss ((ooppttiioonn)) LLAANN eennvviirroonnmmeenntt Wi-Fi radio communication IPv4 only NNoottee Not applicable Static DHCP Wi-Fi radio IP allocation If Static - Unique IP address will be required for each Wi-Fi radio MAC address If DHCP and not using a DNS name - Each Wi-Fi radio MAC address will need a reserved IP address If DHCP and using a DNS name - It is required to create a unique name for each Wi-Fi radio MAC address for Wi-Fi radio management Stryker recommends using the Wi-Fi radio host name when the Wi-Fi radio connects to the wireless network - Example:

SYK-00197b12365 so it may look like http://SYK-

00197b12365.hosp.org iiBBeedd Server IP allocation Static IP required Not applicable VLAN New, existing Install Wi-Fi radio on a separate VLAN IIPP ttrraaffffiicc eennvviirroonnmmeenntt SSoouurrccee iiBBeedd Server Wi-Fi radio PPrroottooccooll // PPoorrtt nnuummbbeerr TCP/80/443 TCP/80/443 CCuussttoommeerr WWLLAANN eennvviirroonnmmeenntt Supported wireless vendors Cisco, Aruba Access point (AP) types Controller-based or autonomous Channel width 2.4 GHz: 20 MHz 5 GHz: 20/40 MHz Channel utilization Consistently less than 30%

Recommended Signal strength range (minimum) Minimum SNR Priority queuing Client exclusion Client load balancing 2.4 GHz: -67dBm +0/-8dBm 5 GHz: -67dBm +0/-8dBm (MedSurg only) Minimum 20dB Prioritized over best effort traffic Recommended Disabled Disabled Recommended Recommended DDeessttiinnaattiioonn Wi-Fi radio iiBBeedd Server RReeqquuiirreedd Yes Yes Yes Yes Yes 3009-009-001 Rev A.0 11 EN CCuussttoommeerr WWLLAANN eennvviirroonnmmeenntt Max number of SSIDs 5 Authentication timeouts Add session timeout of at least 24 hours RReeqquuiirreedd Recommended Recommended NNoottee -- A transmit power asymmetry problem may arise at the edges of virtual cell coverage if an APs transmit power is higher than the Wi-Fi radio (~6 mW 2.4 GHz or 12 mW 5 GHz). Verify the received signal strength indicator (RSSI) of the Wi-Fi radio on the AP. The Wi-Fi radio should never drop below an RSSI of -75 dBm on the AP. PPrroodduucctt iilllluussttrraattiioonn FFiigguurree 11 MMooddeell 33000099 PPrrooCCuuiittyy bbeedd sseerriieess A B C D E F G H I Headboard Operator control panel Patient storage Patient control panel Siderail Support surface Footboard Footboard control panel Integrated pump rack J K L M N O P Q Auxiliary outlet Brake/steer pedal Foley bag hook CPR release handle Siderail release Mattress retainer Caster Traction socket EN 12 3009-009-001 Rev A.0 ABCDEFGHIJKLMNOPQ AApppplliieedd ppaarrttss FFiigguurree 22 TTyyppee BB aapppplliieedd ppaarrttss Contact Stryker Customer Service or Technical Support at: 1-800-327-0770. CCoonnttaacctt iinnffoorrmmaattiioonn Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA NNoottee -- The user and/or the patient should report any serious product-related incident to both the manufacturer and the Competent authority of the European Member State where the user and/or patient is established. To view your operations or maintenance manual online, see https://techweb.stryker.com/. Have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical Support. Include the serial number in all written communication. SSeerriiaall nnuummbbeerr llooccaattiioonn You can find the serial number (A) below the headboard at the head of the bed (TBD). 3009-009-001 Rev A.0 13 EN SSeettuupp comes on.

(page 18)).

(page 19)). WWAARRNNIINNGG -- Always plug the product into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade wall outlet. This product is equipped with a hospital-grade plug for protection against electric shock hazard. CCAAUUTTIIOONN -- Do not clean, disinfect, service, or perform maintenance while the product is in use. NNoottee -- Allow the product to reach room temperature before you conduct any setup or test functional operations. To setup and test the functionality of the product:

1. Plug the product into a grounded, hospital grade wall outlet and make sure that the display at the foot end of the product 2. Siderails raise, lower, lock in the up position, and lock in the intermediate position when lowered (Raisingthesiderails

(page 20), Loweringthesiderails (page 20)). 3. Apply the brake. Push on the product to make sure that all four casters are locked (Applyingorreleasingthebrakes NNoottee -- The BBrraakkee icon (H) located on the footboard control panel (Footboardcontrolpanel-Menucontrols (page 24)) illuminates when the brakes are applied. 4. Release the brake. Push on the product to make sure that all four casters are unlocked. 5. Raise the Fowler (head of bed) to approximately 60. 6. Pull the CPR release handle to make sure that the back will drop with minimal effort (ActivatingtheCPRreleasehandle 7. Perform each function on the footboard control panel to make sure that each function works (Footboardcontrolpanel-

Menucontrols (page 24), Footboardcontrolpanel-Position (page 25)). 8. Perform each function on each control panel on the head end siderails to make sure that each function works (Operator controlpanel,basic,outsidesiderail (page 21), Operatorcontrolpanel,advanced,outsidesiderail(option) (page 22)). 9. Activate the motion stop system. Press BBeedd hheeiigghhtt ddoowwnn (J) (Footboardcontrolpanel-Position (page 25)) to lower the litter. As the litter lowers, push up on the motion interrupt pan under the litter to make sure that downward motion stops. Release the pan and allow downward motion to continue. SSeettttiinngg uupp iiBBeedd WWiirreelleessss ((ooppttiioonn)) WWAARRNNIINNGG -- Always map the iiBBeedd Locator or SSeeccuurree Connect Locator to the location to provide location information. If you move an iiBBeedd Locator or SSeeccuurree Connect Locator after it has been set up and mapped, you must remap to the new location. To setup your product to receive a wireless connection, you must set up the iiBBeedd Locator or SSeeccuurree Connect Locator on the wall at the head end of the product. The iiBBeedd Locator or SSeeccuurree Connect Locator communicates with the product. For instructions about how to mount the iiBBeedd Locator or SSeeccuurree Connect Locator, see the instructions for use included with your optional iiBBeedd Locator or SSeeccuurree Connect Locator. Contact Stryker Technical Support at (800) 327-0770 with any set up questions. NNoottee -- You must load the wireless connection settings before the device will communicate with the iiBBeedd Server application. See the iiBBeedd Server Installation/Configuration Manual. SSeettttiinngg uupp wwiirreedd nnuurrssee ccaallll ccoommmmuunniiccaattiioonn WWAARRNNIINNGG -- Always use a Stryker supplied interface cable. Use of any other cable may cause the product to not function as intended, which may result in patient or user injury. EN 14 3009-009-001 Rev A.0 To setup nurse call communication:

NNoottee -- The product is equipped with an input that accepts a DB-37 nurse call cable. 1. Plug the interface cable into the 37-pin connector on the litter frame at the head end of the product (A) (Figure 3). NNoottee -- Only connect the 37-pin connector to the 37-pin connection on the product or the product Communications Tester (sold separately). 2. Plug the interface cable into the applicable connection (patient station, head wall, or docker station). 3. Press the NNuurrssee ccaallll button (B) to verify the connection between the products nurse call signal and the hospitals nurse call system (Operatorcontrolpanel,basic,outsidesiderail (page 21), Operatorcontrolpanel,advanced,outsidesiderail

(option) (page 22)). To activate nurse call communication, see Activatingnursecall (page 21). SSeettttiinngg uupp wwiirreelleessss nnuurrssee ccaallll ccoommmmuunniiccaattiioonn FFiigguurree 33 3377--ppiinn ccoonnnneeccttoorr TBD 1. 3009-009-001 Rev A.0 15 EN OOppeerraattiioonn PPlluuggggiinngg oorr uunnpplluuggggiinngg tthhee pprroodduucctt WWAARRNNIINNGG Always connect this product to a supply mains with protective earth to avoid the risk of electric shock. Always make sure the product is connected to an appropriate power source if the loss of power would result in unacceptable risk. Always allow enough clearance between the head end of the product and the adjacent wall, so you can unplug the power cord from the wall outlet. Always store the power cord before you transport the product. To plug in the product, plug the power cord into a hospital grade protective earthed outlet. To unplug the product, grasp the mold near the outlet and pull in a direction parallel to the floor (not at an angle). CChhaarrggiinngg tthhee bbaatttteerryy WWAARRNNIINNGG Always disconnect the power cord from the wall outlet if you detect overheating of the battery, cables, or cords. Do not use the product until it has been inspected, serviced, and confirmed to work as intended by maintenance personnel. Always replace the battery after it surpasses its expected service life. Do not open the battery. Do not expose the battery to excessive heat. Do not spill liquid onto the battery or submerge the battery in liquid. CCAAUUTTIIOONN Always plug the product into a hospital grade protective earthed outlet when not in use to maintain a sufficient battery charge and to maximize product performance while operating on battery power. Always replace batteries that have corrosion at the terminals, display cracking, have expanded or bulging sides, or no Always use authorized batteries when you replace the batteries. Use of unauthorized batteries may lead to longer can maintain a full charge. unpredictable system performance. This product is equipped with a battery backup system that charges when the product is plugged into a wall outlet. The battery backup system allows the operator to use the product when the product is unplugged, during a power failure, or during transport. Battery backup functionality activates when you unplug the product. Always check battery backup function. Replace the battery if it does not perform as intended during preventive maintenance. To charge the battery, connect the product to a hospital grade protective earthed outlet. The battery has a full charge within eight hours. EN 16 3009-009-001 Rev A.0 SSttoorriinngg tthhee ppoowweerr ccoorrdd WWAARRNNIINNGG Always store the power cord before you transport the product. Always store the power cord to avoid the risk of entanglement, damage to the power cord, or potential shock hazards. If the power cord is damaged, remove the product from service. CCAAUUTTIIOONN -- Do not pinch the power cord in the bed frame. To store the power cord and auxiliary cord, wrap the cords and secure them with the cord wrap (A) under the head end of the product (Figure 4). TTrraannssppoorrttiinngg tthhee pprroodduucctt FFiigguurree 44 SSttoorriinngg tthhee ppoowweerr ccoorrdd WWAARRNNIINNGG Always use two people when you transport the product. Always store the power cord before you transport the product. Always lock the siderails in the full up position with the sleep surface horizontal when you transport a patient. Always keep limbs, hands, fingers, and other body parts clear of mechanisms and gaps. Always make sure that there are no obstacles near the product. Injury to the patient, operator, bystanders or damage to the frame or surrounding equipment could occur if you collide with an obstacle. Do not attempt to transport the product laterally. This may cause the product to tip. CCAAUUTTIIOONN Do not use the siderails as a push or pull device. Always move the product using the integrated handles in the headboard and footboard. Always remove the patient helper before you transport the product. Do not use the patient helper as a push or pull device. Do not use the oxygen bottle holder as a push or pull device. Do not use the IV pole as a push or pull device. Always make sure that the IV pole is at a low height during transport. 1. Lock the siderail control panel functions (Footboardcontrolpanel-MotionLock (page 26)). To transport the product:

2. Unplug the power cord from the wall outlet. 3. See Storingthepowercord (page 17). 4. Lower the IV pole (RaisingorloweringtheIVpole(option) (page 33)). 5. Turn the oxygen bottle holder in toward the product. 6. Raise and lock the siderails in the full up position (Raisingthesiderails (page 20)). 7. Release the brakes (Applyingorreleasingthebrakes (page 18)). 8. Push the product from the headboard or footboard. 3009-009-001 Rev A.0 17 EN AAppppllyyiinngg oorr rreelleeaassiinngg tthhee bbrraakkeess WWAARRNNIINNGG Always apply the brakes when a patient is getting into or out of the product to avoid instability. Always apply the brakes when the patient is unattended. Do not apply the brakes to slow or stop the product while the product is in motion. You can find the brake pedals at the head end and foot end of the product. To apply the brakes, depress the red side of the pedal (Figure 5). The brake pedal locks all four casters to hold the product in place. To release the brakes, depress the green side of the pedal until the pedal is in the neutral position (Figure 6). This releases all four casters and allows you to move the product. To apply or release the brakes with the electric brake option, press the BBrraakkee button (O) on the operator control panel

(Operatorcontrolpanel,advanced,outsidesiderail(option) (page 22)) or press the BBrraakkee icon (H) on the footboard control panel (Footboardcontrolpanel-Menucontrols (page 24)). NNoottee -- The BBrraakkee icon (I, O) on the operator control panel (Operatorcontrolpanel,basic,outsidesiderail (page 21), Operatorcontrolpanel,advanced,outsidesiderail(option) (page 22)) and the BBrraakkee icon (H) on the footboard control panel

(Footboardcontrolpanel-Menucontrols (page 24)) illuminates when you release the brakes. FFiigguurree 55 AAppppllyyiinngg tthhee bbrraakkeess FFiigguurree 66 RReelleeaassiinngg tthhee bbrraakkeess//nneeuuttrraall ppoossiittiioonn AAppppllyyiinngg oorr rreelleeaassiinngg sstteeeerr lloocckk WWAARRNNIINNGG Always lock the siderails in the full up position with the sleep surface horizontal when you transport a patient. Always unplug the power cord before you transport the product. Always release the brakes before you transport the product. Do not transport the product with the brakes applied. Do not transport the product laterally after you apply the steer lock pedal. The product cannot swivel when you transport with steer lock. Do not attempt to release steer lock while the product is in motion. Steer lock guides the product along a straight line when you transport and pivot the product around corners. The steer lock pedal locks the casters on the foot end. The steer lock pedal is at both the head end and foot end of the product. To transport with steer lock:

1. Align the casters to face the direction of transport. 2. To apply the steer caster, depress the green side of the pedal (Figure 7). To release steer lock, depress the red side of the pedal until the pedal is in the neutral position (Figure 8). NNoottee -- To move the product in any direction, release the steer lock pedal. EN 18 3009-009-001 Rev A.0 FFiigguurree 77 AAppppllyyiinngg sstteeeerr lloocckk FFiigguurree 88 RReelleeaassiinngg sstteeeerr lloocckk//nneeuuttrraall ppoossiittiioonn AAccttiivvaattiinngg tthhee CCPPRR rreelleeaassee hhaannddllee CCAAUUTTIIOONN -- Always make sure that all persons and equipment are away from the area below and around the Fowler before you activate the CPR release handle. The CPR release handle is for emergency use only. When you raise the Fowler and need quick access to the patient, pull the CPR release handle to position the product to 0. The two CPR release handles are on the left and right side of the litter Gatch section (A) (Figure 9). To pull the CPR release handle:

1. Pull the handle (A) on the left or right side of the litter Gatch section (Figure 9). NNoottee -- Release the CPR release handle at any time to stop product Fowler, Gatch, and foot section motion. 2. Guide the Fowler to the flat position. NNoottee -- When you pull the CPR release handle, the Gatch and foot section lower. FFiigguurree 99 AAccttiivvaattiinngg tthhee CCPPRR rreelleeaassee hhaannddllee RReemmoovviinngg oorr rreeppllaacciinngg tthhee hheeaaddbbooaarrdd WWAARRNNIINNGG -- Do not use the headboard for CPR support. You can remove the headboard (A) (Productillustration (page 12)) to access the patient or to clean the product. 1. Grasp the handles and lift the headboard straight up and off the product. To remove the headboard:

To replace the headboard:

1. Align the headboard pegs with the sockets at the head end of the product. 2. Lower the headboard until the headboard seats into the sockets. 3009-009-001 Rev A.0 19 EN RReemmoovviinngg oorr rreeppllaacciinngg tthhee ffoooottbbooaarrdd You can remove the footboard (G) (Productillustration (page 12)) to access the patient or to clean the product. 1. Grasp the handles and lift the footboard straight up and off the product. To remove the footboard:

To replace the footboard:

1. Align the footboard pegs with the sockets at the foot end of the product. 2. Lower the footboard until the footboard seats into the sockets. RRaaiissiinngg tthhee ssiiddeerraaiillss WWAARRNNIINNGG Always set the siderail position for appropriate patient safety. Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts of the product. NNoottee -- Do not use siderails as a patient restraint device. When you raise the siderails, listen for a click to indicate that the siderail locks into position. Pull on the siderail to make sure the siderail locks. To raise the siderail to the highest position, press and hold the siderail release (N) (Productillustration (page 12)) and rotate the siderail up from either the lowest position or intermediate position (Figure 10). To raise the siderail to the intermediate position, grasp and rotate the siderail up from the lowest position until you hear the siderail click (Figure 11). FFiigguurree 1100 SSiiddeerraaiill hhiigghheesstt ppoossiittiioonn LLoowweerriinngg tthhee ssiiddeerraaiillss FFiigguurree 1111 SSiiddeerraaiill iinntteerrmmeeddiiaattee ppoossiittiioonn WWAARRNNIINNGG Always set the siderail position for appropriate patient safety. Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts of the product. NNoottee -- Do not use siderails as a patient restraint device. When you lower the siderails, listen for a click to indicate that the siderail locks into position. Pull on the siderail to make sure the siderail locks. To lower the siderail to the intermediate position, press the siderail release (N) (Productillustration (page 12)) and rotate the siderail forward until the siderail stops at the intermediate position (Figure 11). To lower the siderail to its lowest position, press and hold the siderail release and rotate the siderail to the lowest position (Figure 12). EN 20 3009-009-001 Rev A.0 FFiigguurree 1122 SSiiddeerraaiill lloowweesstt ppoossiittiioonn SSeeccuurriinngg aa FFoolleeyy bbaagg ttoo tthhee FFoolleeyy bbaagg hhooookk NNoottee The safe working load of the Foley bag hook is 10 lb (4.5 kg). Do not allow the Foley bag to touch the ground while the product is in low height. There are two Foley bag hooks under the foot section (L) (Productillustration (page 12)), one on either side of the product. To secure a Foley bag, place the hook of the Foley bag on the Foley bag hook. AAccttiivvaattiinngg nnuurrssee ccaallll Nurse call allows the patient or healthcare professional to send a signal to the nurse station for assistance. To activate nurse call, press the NNuurrssee ccaallll button (B) (Operatorcontrolpanel,basic,outsidesiderail (page 21), Operator controlpanel,advanced,outsidesiderail(option) (page 22)) (A) (Patientcontrolpanel,insidesiderail (page 23)). NNoottee -- Nurse call requires a connection between the product and an applicable input (patient station, head wall, or docker station). See Settingupwirednursecallcommunication (page 14). CCoonnnneeccttiinngg ppeerriipphheerraall eeqquuiippmmeenntt ttoo tthhee aauuxxiilliiaarryy oouuttlleett WWAARRNNIINNGG Only use hospital grade electric equipment consuming 5A or less with the auxiliary outlet. The use of standard electric equipment may bring the current leakage to a level unacceptable for hospital equipment. Do not use the auxiliary outlet for life sustaining equipment. The auxiliary outlet is a built-in outlet for peripheral equipment. The auxiliary outlet (J) is at the foot end of the product

(Productillustration (page 12)). NNoottee -- Resettable circuit breakers at the head end of the product protect the auxiliary outlet. OOppeerraattoorr ccoonnttrrooll ppaanneell,, bbaassiicc,, oouuttssiiddee ssiiddeerraaiill WWAARRNNIINNGG Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts falls. of the product. CCAAUUTTIIOONN -- Always make sure that the product is clear of obstacles before you use motion functions. NNoottee -- The motion button flashes when the product reaches the motion limit. 3009-009-001 Rev A.0 21 EN A B C D E F G H I J Bed exit Nurse call Gatch up Gatch down Fowler up Fowler down Fowler 30+

Bed height up Bed height down Brake indicator Press and hold to cancel bed exit alarm Activates nurse call Raises the Gatch Lowers the Gatch Raises the Fowler Lowers the Fowler Raises the litter Lowers the litter Illuminates when the Fowler is 30+

Illuminates when you apply or release the brake OOppeerraattoorr ccoonnttrrooll ppaanneell,, aaddvvaanncceedd,, oouuttssiiddee ssiiddeerraaiill ((ooppttiioonn)) WWAARRNNIINNGG Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts falls. of the product. CCAAUUTTIIOONN -- Always make sure that the product is clear of obstacles before you use motion functions. NNoottee -- The motion button flashes when the product reaches the motion limit. A B Bed exit Nurse call Press and hold to cancel bed exit alarm Activates nurse call EN 22 3009-009-001 Rev A.0 C D E F G H I J K L M N O P Patient ingress/egress Cardiac chair position Vascular position Trendelenburg Bed flat Reverse Trendelenburg Gatch up Gatch down Fowler up Fowler down Fowler 30+

Bed height up Bed height down Brake indicator Places the product into a position for patient ingress or egress NNoottee -- The patient ingress or egress button disables bed exit. Places the product into the cardiac chair position Places the product into the vascular position Places the product into the Trendelenburg position

(head down with foot up) Places the product into a 0 horizontal position Places the product into the Reverse Trendelenburg position (head up with foot down) Raises the Gatch Lowers the Gatch Raises the Fowler Lowers the Fowler Raises the litter Lowers the litter Illuminates when the Fowler is 30+

Illuminates when you apply or release the brake PPaattiieenntt ccoonnttrrooll ppaanneell,, iinnssiiddee ssiiddeerraaiill WWAARRNNIINNGG Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient Always lock the controls when the patient is unattended. Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts falls. of the product. CCAAUUTTIIOONN -- Always make sure that the product is clear of obstacles before you use motion functions. Healthcare professionals must instruct patients how to operate the patient control panel. A B C Nurse call Fowler up Fowler down Activates nurse call Raises the Fowler Lowers the Fowler 3009-009-001 Rev A.0 23 EN D E Gatch up Gatch down Raises the Gatch Lowers the Gatch PPeennddaanntt,, bbaassiicc ((ooppttiioonn)) TBD TBD Healthcare professionals must instruct patients how to operate the pendant. PPeennddaanntt,, aaddvvaanncceedd ((ooppttiioonn)) Healthcare professionals must instruct patients how to operate the pendant. FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- MMeennuu ccoonnttrroollss The menu controls are located on the touch panel of the footboard. Press the icons to display the functions of the product. A B C D E F Screen Bed exit iiBBeedd Watch Scale Position Motion Lock Displays menu functions Activates and displays bed exit functions (Footboardcontrolpanel-Bed exit (page 29)) Activates and displays iiBBeedd Watch functions (Footboardcontrolpanel-

iiBBeeddWatch (page 30)) Displays scale functions (Footboardcontrolpanel-Scale (page 26)) Displays position functions (Footboardcontrolpanel-Position (page 25)) Displays lockout functions (Footboardcontrolpanel-MotionLock (page 26)) EN 24 3009-009-001 Rev A.0 G H Settings Brake Displays settings (Footboardcontrolpanel-Settings (page 31)) Basic - Displays brake lock status Advanced (option) - Apply or release the brakes (Applyingorreleasing thebrakes (page 18)) FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- PPoossiittiioonn WWAARRNNIINNGG Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient Always make sure that cables, wires, and tubing from other equipment are routed so that they are not pinched by parts falls. of the product. CCAAUUTTIIOONN -- Always make sure that the product is clear of obstacles before you use motion functions. The PPoossiittiioonn screen displays the position functions of the product. A B C D E F G H I J K L Home Bed flat Fowler up Fowler down Gatch up Gatch down Bed height up Bed height down Trendelenburg Reverse Trendelenburg Returns to the HHoommee screen (see Footboardcontrol panel-Menucontrols (page 24)) Low Height Range settings Returns to the LLooww HHeeiigghhtt RRaannggee screen Cardiac chair position Places the product into the cardiac chair position Places the product into a 0 horizontal position Raises the Fowler Lowers the Fowler Raises the Gatch Lowers the Gatch Raises the litter Lowers the litter Places the product into the Trendelenburg position

(head down with foot up) Places the product into the Reverse Trendelenburg position (head up with foot down) 3009-009-001 Rev A.0 25 EN M N Vascular position Back Places the product into the vascular position Returns to the PPoossiittiioonn screen FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- MMoottiioonn LLoocckk WWAARRNNIINNGG Always lock the controls when the patient is unattended. Always lock the controls when the patient's condition requires extra safety measures. The MMoottiioonn LLoocckk screen displays the lockout functions of the product. Lockouts can lock out motion control input from the operator control panel and patient control panel. NNoottee -- Bed exit, scale, and nurse call features are still available. Home Returns to the HHoommee screen (Footboardcontrolpanel-Menucontrols

(page 24)) A B C D E F G H Screen lock Returns to the SSccrreeeenn LLoocckk screen Head (Fowler) lock Lock or unlock head (Fowler) controls 30+ (Fowler) lock Lock or unlock the head (Fowler) position to 30+

Knee (Gatch) lock Lock or unlock knee (Gatch) controls Bed height lock Lock or unlock bed height controls Lock all Back Lock or unlock all motion function Returns to the MMoottiioonn LLoocckk screen NNoottee The CPR release handle overrides all lockouts. Lock parameters are saved when you unplug the product. Do not lock control panel functions if you must access control panel functions when you remove the footboard. If the product is in a specific position when you enable a lock, the product will be locked in that position. FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- SSccaallee The SSccaallee screen displays the scale functions of the product. EN 26 3009-009-001 Rev A.0 A Home B Info C Save Weight Zero (Non-NAWI) Tare (NAWI) Add Equip. D E F Scale History Returns to the HHoommee screen (Footboardcontrolpanel-

Menucontrols (page 24)) Displays the SSccaallee IInnffoo screen Select to save the current displayed weight (Weighinga patient (page 28)) Select to zero/tare the scale or set the scale for a new patient (Zeroing/taringthescale (page 27)) Select to add or remove equipment (Addingorremoving equipment (page 28)) Indicates how many items have been added to bed Displays the SSccaallee HHiissttoorryy screen NNoottee -- The SSccaallee HHiissttoorryy stores up to 40 scale readings. G Weight change indicator Displays an up or down arrow to indicate weight change H Exit Returns to the SSccaallee screen ZZeerrooiinngg//ttaarriinngg tthhee ssccaallee Before you place a patient on the product, make sure that you zero/tare the scale. NNoottee ZZeerroo will display for non-NAWI and TTaarree will display for NAWI. Always zero/tare the scale after adding a support surface, mattress, or linens to the bed frame. To zero/tare the scale:

1. Press the SSccaallee button (D) on the footboard control panel (Footboardcontrolpanel-Menucontrols (page 24)). 2. On the SSccaallee screen, press the ZZeerroo//TTaarree button (D) (Footboardcontrolpanel-Scale (page 26)). 3. On the NNeeww PPaattiieenntt?? screen, you may choose from the following:

YYeess, to zero/tare and delete scale history. NNoo, to zero/tare and not delete scale history. CCaanncceell, to cancel zero/tare and return to the SSccaallee screen. NNoottee -- Do not touch the product when you zero/tare the scale. 3009-009-001 Rev A.0 27 EN WWeeiigghhiinngg aa ppaattiieenntt WWAARRNNIINNGG Do not use the scale system reading as a reference for medical treatment. The scale system assists only to monitor the patients weight variation. Before you place a patient on the product, make sure that you zero/tare the scale (Zeroing/taringthescale (page 27)). NNoottee -- Always zero/tare the scale after you add a support surface, mattress, or linens to the product. To weigh a patient:

1. Press the SSccaallee button (D) on the footboard control panel (Footboardcontrolpanel-Menucontrols (page 24)). 2. On the SSccaallee screen, press the SSaavvee WWeeiigghhtt button (C) (Footboardcontrolpanel-Scale (page 26)). NNoottee -- Do not touch the product when you weigh the patient. The SSccaallee IInnffoo screen will display when the last weight was taken on the LLaasstt WWeeiigghh line (Footboardcontrolpanel-Scale

(page 26)). NNoottee -- The previous weight from the LLaasstt WWeeiigghh line will appear in SSccaallee HHiissttoorryy (F) (Footboardcontrolpanel-Scale

(page 26)) AAddddiinngg oorr rreemmoovviinngg eeqquuiippmmeenntt NNoottee -- The add or remove equipment function is only available when there is TBD lb/kg gain/loss. A B C D E Home Info Return Reset Save Returns to the HHoommee screen (Footboardcontrolpanel

-Menucontrols (page 24)) Displays the SSccaallee IInnffoo screen (Footboardcontrol panel-Scale (page 26)) Returns to the SSccaallee screen (Footboardcontrolpanel

-Scale (page 26)) Select to reset the added equipment to zero Select to save the current displayed weight as equipment EN 28 3009-009-001 Rev A.0 To add or remove equipment:

1. Press the SSccaallee button (D) on the footboard control panel (Footboardcontrolpanel-Menucontrols (page 24)). 2. On the SSccaallee screen, press the AAdddd EEqquuiipp.. button (E) (Footboardcontrolpanel-Scale (page 26)). 3. One item at a time, add or remove the desired equipment from the product. NNoottee -- Do not touch the product while the product weighs the equipment. 4. Press the SSaavvee button to save the current weight and equipment count. FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- BBeedd eexxiitt The BBeedd EExxiitt screen displays the bed exit functions of the product. A B C D E Home Low Medium High Turn off Returns to the HHoommee screen (Footboardcontrol panel-Menucontrols (page 24)) Allows the patient to move freely on the bed. Alarms when the patient moves 50 percent body weight out of the designated zone. Allows for limited movement. Alarms when the patient approaches the siderail or the foot end of the bed. Allows minimal movement. Alarms when the patient moves out of the tightly restricted zone. Turns off bed exit AArrmmiinngg oorr ddiissaarrmmiinngg bbeedd eexxiitt WWAARRNNIINNGG -- Do not use bed exit to replace patient monitoring protocol, it is intended only to aid in the detection of a patient exiting the product. When armed, bed exit monitors the patients position on the product. To arm bed exit:

1. Set the scale to zero/tare if not already performed. See Zeroing/taringthescale (page 27) 3009-009-001 Rev A.0 29 EN NNoottee -- If you do not set the scale to zero before you place a patient on the product, bed exit may not operate as intended. 2. Position the patient on the product.

(page 24)). 3. Press the BBeedd EExxiitt button (B) on the footboard control panel to arm bed exit (Footboardcontrolpanel-Menucontrols 4. Select the desired zone (B, C, D) (Footboardcontrolpanel-Bedexit (page 29)). If you change the parameter conditions for bed exit:

Bed exit priority signal sent (Settingupwirednursecallcommunication (page 14)) LEDs on the footboard and siderails flash red Sound alarm is triggered To disarm bed exit, press TTuurrnn OOffff (E) (Footboardcontrolpanel-Bedexit (page 29)). FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- iiBBeedd WWaattcchh The iiBBeedd WWaattcchh screen displays the iiBBeedd Watch functions of the product. When enabled, iiBBeedd Watch alerts when changes are made to the selected bed settings:

Low height Siderails up Head angle Bed flat A B C D E F G H Home Info Low Height Head right siderail Head left siderail Foot right siderail Foot left siderail Head Angle Returns to the HHoommee screen (Footboardcontrol panel-Menucontrols (page 24)) Displays the iiBBeedd WWaattcchh IInnffoo screen Monitor low height of the bed Monitor the head right siderail in the highest position Monitor the head left siderail in the highest position Monitor the foot right siderail in the highest position Monitor the foot left siderail in the highest position Monitor the head angle of the bed EN 30 3009-009-001 Rev A.0 I J K Bed Flat Turn Off Exit Monitor the bed flat position Turn off iiBBeedd Watch Returns to the iiBBeedd WWaattcchh OOnn screen 2. Press the iiBBeedd WWaattcchh button (C) on the footboard control panel to enable iiBBeedd Watch (Footboardcontrolpanel-Menu EEnnaabblliinngg oorr ddiissaabblliinngg iiBBeedd WWaattcchh To enable iiBBeedd Watch:

1. Position the patient on the product. controls (page 24)). 3. Select the desired bed settings to monitor (Footboardcontrolpanel-iiBBeeddWatch (page 30)). If you change the monitored settings for iiBBeedd Watch, the following can occur:

Bed exit priority signal sent (Settingupwirednursecallcommunication (page 14)) LEDs on the footboard and siderails flash red Sound alarm is triggered To disable iiBBeedd Watch, press TTuurrnn OOffff (J) (Footboardcontrolpanel-iiBBeeddWatch (page 30)). FFoooottbbooaarrdd ccoonnttrrooll ppaanneell -- SSeettttiinnggss The SSeettttiinnggss screen displays the settings available to view or change for the product. A B C D E Home History Night Light Help Service Returns to the HHoommee screen (Footboardcontrolpanel-Menucontrols

(page 24)) Displays the SSccaallee HHiissttoorryy screen Select to toggle through the following: Night light on, night light automatic, night light off Displays a QR code and web address for further information Displays service info, options to view current bed configuration, and error codes 3009-009-001 Rev A.0 31 EN Settings Displays settings Displays advanced settings F G Advanced AAddvvaanncceedd SSeettttiinnggss NNoottee -- Press and hold the SSeettttiinnggss button (F) to display the advanced settings button. Lighting Select to adjust the display brightness or set to automatic Low height range Select to toggle the low height range of the product Scale info Wi-Fi info Displays the current software version, local gravity, and calibrated gravity Displays the MAC address, connection type, IP address, SSID, signal strength, and BSSID iiBBeedd Locator Displays the locator ID and locator battery status Set time format Select to toggle between a 12hr or 24hr time format EN 32 3009-009-001 Rev A.0 AAcccceessssoorriieess aanndd ppaarrttss These accessories and parts may be available for use with your product. Confirm availability for your configuration or region. NNaammee Battery Bed extender 2-stage IV pole, single 2-stage IV pole, dual Line management (pack of 70) Patient helper bracket ZZiimmmmeerr patient helper bracket Pendant, basic Pendant, advanced Upright oxygen bottle holder Upright oxygen bottle holder NNuummbbeerr 700000341245 TBD 300900350100 300900350200 300900450010 300900450100 300900450105 300900470100 300900470200 300900450050 300900450150 RRaaiissiinngg oorr lloowweerriinngg tthhee IIVV ppoollee ((ooppttiioonn)) CCAAUUTTIIOONN Do not load the IV pole above the safe working load of 40 lb (18 kg). Do not load an individual IV pole hook above the safe working load of 20 lb (9 kg). Do not use the IV pole as a push or pull device. To position the IV pole:

position (Figure 13). 1. Lift and pivot the IV pole from the storage position and push down until the IV pole locks into the receptacle. 2. To raise the height of the pole, pull up on the telescoping portion (A) of the pole until it locks into place at the fully raised 3. Rotate the IV hangers (B) to the desired position and hang the IV bags (Figure 13). 4. To lower the pole, turn the latch (C) clockwise until the telescoping portion (A) lowers into the bottom tube (Figure 13). 5. Lift up and pivot the pole down into the storage position. 3009-009-001 Rev A.0 33 EN AAttttaacchhiinngg oorr rreemmoovviinngg tthhee ppaattiieenntt hheellppeerr ((ooppttiioonn)) FFiigguurree 1133 TTwwoo--ssttaaggee IIVV ppoollee WWAARRNNIINNGG -- Always use two people to attach or remove the patient helper. CCAAUUTTIIOONN Always secure the lifting pole in the mounting bracket before you adjust the patient helper. Always remove the patient helper before you transport the product. You can attach the patient helper into the patient helper mounting bracket at the head end of the product. To attach the patient helper:

1. Insert the lifting pole (A) into the mounting bracket (B) (Figure 14). 2. Rotate the lifting pole in the mounting bracket until the patient helper knob (C) locks in position (Figure 14). EN 34 3009-009-001 Rev A.0 ABC FFiigguurree 1144 AAttttaacchhiinngg oorr rreemmoovviinngg tthhee ppaattiieenntt hheellppeerr Reverse steps to remove the patient helper. AAddjjuussttiinngg tthhee ppaattiieenntt hheellppeerr ((ooppttiioonn)) WWAARRNNIINNGG -- Do not load the patient helper above the safe working load of 200 lb (90.7 kg). CCAAUUTTIIOONN Always secure the lifting pole in the mounting bracket before you adjust the patient helper. Do not use the patient helper as a push or pull device. Always make sure that the patient helper mounting bracket is secure before use. The patient helper assists the patient to change position in bed. To adjust the patient helper:

1. Pull the patient helper knob (A) and rotate the lifting pole (B) until the desired position (Figure 15). 2. Release the patient helper knob (A) and rotate the lifting pole (B) until the knob locks in position (Figure 15). 3. Lift the trapeze hanger bracket (C) and move it forward or backward until the desired position (Figure 15). NNoottee -- Make sure that the trapeze hanger is secure in one of the keyed positions on the lifting pole. 3009-009-001 Rev A.0 35 EN ABC AAttttaacchhiinngg tthhee ooxxyyggeenn bboottttllee hhoollddeerr FFiigguurree 1155 AAddjjuussttiinngg tthhee ppaattiieenntt hheellppeerr CCAAUUTTIIOONN Do not load the oxygen bottle holder above the safe working load of TBD lb. Do not use the oxygen bottle holder as a push or pull device. To attach the oxygen bottle holder:

1. Insert the oxygen bottle holder support bar into the accessory socket that is located on either side of the product at the head end and foot end. EN 36 3009-009-001 Rev A.0 BAC CClleeaanniinngg aanndd ddiissiinnffeeccttiinngg wwiitthh wwiippeess For United States only. Confirm availability for your configuration or region. Call Stryker Customer Service: 1-800-327-

0770. Strykers preferred wipes (2060-000-001 6'' x 10'' or 2060-000-002 9'' x 12'') include the following active ingredients:

n-Alkyl (60% C14, 30% C16, 5% C12, 5% C18) dimethyl benzyl ammonium chloride - 0.154%

n-Alkyl (68% C12, 32% C14) dimethyl ethylbenzyl ammonium chloride - 0.154%

Isopropanol - 21.000%

1. To clean, wipe external surfaces with a fresh, clean wipe to remove all visible soils. Repeat as necessary until the Non-active ingredient: Ethylene Glycol Monobutyl Ether < 3%

NNoottee -- For safety information, read the product label. To clean or disinfect the external product surface:

product is clean. NNoottee Use as many wipes as necessary. Complete step 1 before you disinfect. 2. To disinfect, wipe external surfaces with a fresh, clean wipe until wet. Allow the external surface to remain wet for two minutes at room temperature. 3. Allow the product to dry before you return it to service. 3009-009-001 Rev A.0 37 EN CClleeaanniinngg CCAAUUTTIIOONN Do not clean, disinfect, service, or perform maintenance while the product is in use. Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors. Remove the occupant from the product, clean up the fluid, and inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product. Do not return the product to service until dry and tested for safe operation. Recommended cleaning method:

1. Hand wash all exposed surfaces of the product with a mild detergent by spray or pre-soaked wipes. 2. Follow the cleaning solution manufacturers instructions for appropriate contact time and rinse requirements. 3. Dry the product before you return it to service. NNoottee -- Avoid oversaturation. Do not allow the product to remain wet. EN 38 3009-009-001 Rev A.0 DDiissiinnffeeccttiinngg CCAAUUTTIIOONN Do not clean, disinfect, service, or perform maintenance while the product is in use. Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors. Remove the occupant from the product, clean up the fluid, and inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product. Do not return the product to service until dry and tested for safe operation. Always wipe down with clean water (or 70% isopropyl alcohol, if using VViirreexx TB) and dry each product after disinfecting. Some disinfectants are corrosive in nature and may cause damage to the product. If you do not rinse and dry the product, you may leave a corrosive residue on the surface of the product. This corrosive residue could cause premature degradation of critical components. Failure to follow these disinfecting instructions may void your warranty. Chlorinated bleach solution (10,000 ppm available chlorine, 941 mL of a 5.25% sodium hypochlorite solution per 4000 Recommended disinfectants for this products surfaces include:

Quaternary (active ingredient - ammonium chloride) Phenolic (active ingredient - o-phenylphenol) Alcohol (active ingredient - 70% isopropyl alcohol) Accelerated hydrogen peroxide (5,000 ppm hydrogen peroxide) mL of water) Disinfection method:

1. Follow the disinfectant solution manufacturers dilution recommendations. 2. Apply the recommended disinfectant solution by spray or pre-soaked wipes. 3. Hand wash all exposed surfaces of the product with the recommended disinfectant. 4. Dry the product before you return it to service. NNoottee Avoid oversaturation. Do not allow the product to remain wet. Follow the manufacturers dilution recommendations for appropriate contact time and rinse requirements. Follow the chemical manufacturers guidelines to disinfect. 3009-009-001 Rev A.0 39 EN PPrreevveennttiivvee mmaaiinntteennaannccee Remove the product from service before you perform the preventive maintenance inspection. Check all items listed during annual preventive maintenance for all Stryker Medical products. You may need to perform preventive maintenance checks more often based on your level of product usage. Service only by qualified personnel. NNoottee -- Clean and disinfect the exterior of the support surface before inspection, if applicable. Inspect the following items:

TBD Product serial number:

Completed by:

Date:

EN 40 3009-009-001 Rev A.0 WWiirreelleessss nnoottiiffiiccaattiioonnss For product equipped with optional wireless communication technology, these statements apply to the countries as indicated:

CCoouunnttrryy NNoottiiffiiccaattiioonn Contains IC ID: 4919E-SDMACP Contains IC ID: 5123A-BGTWT32I This device complies with Innovation, Science and Economic Development Canadas license-

exempt RSSs. Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Canada Le prsent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorise aux deux conditions suivantes : (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radiolectrique subi, mme si le brouillage est susceptible d'en compromettre le fonctionnement. Mexico La operacin de este equipo est sujeta a las siguientes dos condiciones: (1) es posible que este equipo o dispositivo no cause interferencia perjudicial y (2) este equipo o dispositivo debe aceptar cualquier interferencia, incluyendo la que pueda causar su operacin no deseada. Contains FCC ID: Z7A-SDMACP Contains FCC ID: QOQWT32I United States This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Changes or modifications not expressly approved by the party responsible for compliance could void the users authority to operate the equipment. Frequency Tolerance: +/-20 ppm 3009-009-001 Rev A.0 41 EN EEMMCC iinnffoorrmmaattiioonn WWAARRNNIINNGG Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be no closer than 12 inches (30 cm) to any part of PPrrooCCuuiittyy bed series, including cables specified by the manufacturer. Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the product. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they operate properly. The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation. The 3009 PPrrooCCuuiittyy bed series was evaluated using the following cables:

CCaabbllee AC mains input cable AC aux input cable AC aux output cable Nurse call (DB-37) USB cable Pendant LLeennggtthh ((mm)) 2.5 2.5 1.8 2.4 4.7 5.3 GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc eemmiissssiioonnss The 3009 PPrrooCCuuiittyy bed series is intended for use in the electromagnetic environment specified below. The customer or the user of the 3009 PPrrooCCuuiittyy bed series should assure that it is used in such an environment. CCoommpplliiaannccee EElleeccttrroommaaggnneettiicc eennvviirroonnmmeenntt EEmmiissssiioonnss tteesstt RF Emissions CISPR 11 RF Emissions CISPR 11 Harmonic Emissions IEC 61000-3-2 Voltage Fluctuations Flicker Emissions IEC 61000-3-3 Group 1 Class A Class A Complies NNoottee -- The emissions characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which CISPR 11 class B is normally required) this equipment might not offer adequate protection to radio-frequency communication services. The user might need to take mitigation measures, such as relocating or re-

orienting the equipment. GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc iimmmmuunniittyy The 3009 PPrrooCCuuiittyy bed series is suitable for use in a professional healthcare facility environment and not in environments exceeding immunity test conditions that the product was evaluated to, such as near high frequency (HF) surgical equipment and inside of the radio frequency (RF) shielded room of magnetic resonance imaging (MRI) equipment. The customer or the user of the 3009 PPrrooCCuuiittyy bed series should assure that it is used in such an environment and that the electromagnetic environment guidance listed below is followed. IImmmmuunniittyy tteesstt IIEECC 6600660011 tteesstt lleevveell CCoommpplliiaannccee lleevveell Electrostatic Discharge

(ESD) IEC 61000-4-2 8 kV contact 15 kV air 8 kV contact 15 kV air EElleeccttrroommaaggnneettiicc eennvviirroonnmmeenntt--gguuiiddaannccee Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. EN 42 3009-009-001 Rev A.0 GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc iimmmmuunniittyy Electrostatic fast transient/

burst IEC 61000-4-4 2 kV for power supply lines 1 kV for input/output lines 2 kV for power supply lines 1 kV for input/output lines Surge IEC 61000-4-5 0.5 kV, 1 kV lines to lines 0.5 kV, 1 kV, 2 kV lines to earth 0.5 kV, 1 kV lines to lines 0.5 kV, 1 kV, 2 kV lines to earth Voltage dips, voltage variations and short interruptions on power supply input lines IEC 61000-4-11 0%UT for 0.5 cycle at 0, 45, 90, 135, 180, 225, 270, and 315 0%UT for 0.5 cycle at 0, 45, 90, 135, 180, 225, 270, and 315 0%UT for 1 cycle 0%UT for 1 cycle 70%UT (30% dip in UT) for 25/30 cycles 70%UT (30% dip in UT) for 25/30 cycles 0% UT for 250/300 cycles 0% UT for 250/300 cycles Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 30 A/m 30 A/m NNoottee -- UT is the a.c. mains voltage before applications of the test level. Main power quality should be that of a typical commercial or hospital environment. Main power quality should be that of a typical commercial or hospital environment. Main power quality should be that of a typical commercial or hospital environment. If the user of the 3009 PPrrooCCuuiittyy bed series requires continued operation during power main interruptions, it is recommended that the device be powered from an uninterrupted power supply or a battery. Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. 3009-009-001 Rev A.0 43 EN Portable and mobile RF communications equipment should follow the guidance in the table titled Recommended separation distances between portable and mobile RF communication equipment and the 3009 PPrrooCCuuiittyy bed series. If the mobile service is not listed in the table, the recommended separation distance should be calculated from the equation appropriate for the frequency of the transmitter. Recommended separation distance D=(2) (P ) where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency rangeb. Interference may occur in the vicinity of equipment marked with the following symbol:

Conducted RF IEC 61000- 4-6 Radiated RF IEC 61000-4-3 3 Vrms 150 kHz to 80 MHz 3 V/m 80 MHz to 2.7 GHz 3 Vrms 3 V/m NNoottee -- These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. NNoottee -- The ISM (Industrial, Scientific, and Medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to 6.795 MHz;

13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz. aField strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the 3009 PPrrooCCuuiittyy bed series is used exceeds the applicable RF compliance level above, the 3009 PPrrooCCuuiittyy bed series should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the 3009 PPrrooCCuuiittyy bed series. bOver the frequency range 150 kHz to 80 MHz, field strengths are less than 3 Vrms. EN 44 3009-009-001 Rev A.0 RReeccoommmmeennddeedd sseeppaarraattiioonn ddiissttaanncceess bbeettwweeeenn ppoorrttaabbllee aanndd mmoobbiillee RRFF ccoommmmuunniiccaattiioonn eeqquuiippmmeenntt aanndd tthhee 33000099 PPrrooCCuuiittyy bbeedd sseerriieess The 3009 PPrrooCCuuiittyy bed series is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the 3009 PPrrooCCuuiittyy bed series can help prevent electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the 3009 PPrrooCCuuiittyy bed series, including cables, as recommended below, according to the maximum output power of the communications equipment. MMaaxxiimmuumm ppoowweerr

((WW)) MMiinniimmuumm sseeppaarraattiioonn ddiissttaannccee

((mm)) BBaanndd ((MMHHzz)) 380-390 430-470 704-787 800-960 1,700-1,990 2,400-2,570 SSeerrvviiccee TETRA 400 GMRS 460;

FRS 460 LTE Band 13, 17 GSM 800/900;

TETRA 800;

iDEN 820;

CDMA 850;

LTE Band 5 GSM 1800;

CDMA 1900;

GSM 1900;

DECT;

LTE Band 1, 3, 4, 25;

UMTS Bluetooth;

WLAN;

802.11 b/g/n;

RFID 2450;

LTE Band 7 1.8 2.0 0.2 2.0 2.0 2.0 0.2 0.3 0.3 0.3 0.3 0.3 0.3 0.3 5,100-5,800 WLAN 802.11 a/n For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters

(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NNoottee -- These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. 3009-009-001 Rev A.0 45 EN Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA 3009-009-001 Rev A.0 WCR: AA.16 2020/05

PPoowweerr--PPRROO 22 CCoott OOppeerraattiioonnss//MMaaiinntteennaannccee MMaannuuaall 650700000000 650700080301 650700450301 650705550001 650705550002 650705550003 6507-009-001 Rev AB.3 2021-08 EN SSyymmbboollss Refer to instruction manual/booklet Consult instructions for use CE mark Authorized representative in the European Community European medical device General warning Caution Warning; crushing of hands Warning; non-ionizing radiation No pushing China RoHS without declarable substances China RoHS with declarable substances Catalogue number Lot (batch) code Serial number For US Patents see www.stryker.com/patents Manufacturer Date of manufacture 6507-009-001 Rev AB.3 EN Importer Mass of equipment with safe working load Safe working load Type BF applied part Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1:2012 and CAN/

CSA-C22.2 No. 60601-1:14. Direct current Alternating current Class II electrical equipment: equipment in which protection against electric shock does not rely on basic insulation only, but in which additional safety precautions such as double insulation or reinforced insulation are provided, there being no provision for protective earthing or reliance upon installation conditions. Dangerous voltage Extend Retract IIPP3366 Ingress protection rating In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic Equipment (WEEE) as amended, this symbol indicates that the product should be collected separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor for disposal information. Ensure infected equipment is decontaminated prior to recycling. The Rechargeable Battery Recycling Corporation (RBRC) is a non-profit, public service organization that promotes the recycling of portable rechargeable batteries. Batteries must be delivered to a battery collection site. Visit the RBRC website (www.rbrc.org) to find a nearby collection site or call the phone number shown on the recycling symbol. Two person lift This way up Fragile, handle with care Keep dry EN 6507-009-001 Rev AB.3 87VL~Stacking limit by number Battery terminal identification (D - data (SMBus data line), C-clock (SMBus clock line), T- T-Pin or temperature, - negative terminal, + positive terminal) 2800 mAh/71.68 Wh Battery capacity and duration Cot duty cycle: 16.7%

English text below this symbol is intended for USA audiences only Distributed by in the US MMAADDEE IINN UU..SS..AA.. Product made in the United States of America Box manufacturers certificate The AAllvvaarriiuumm charger complies with the requirements of UL 62368-1:2019 Ed. 3 and CSA C22.2#62368-1:2019 Ed. 3 for audio/video, information and communication technology equipment, The AAllvvaarriiuumm battery complies with the requirements of UL 62133-2:2020 Ed. 1 and CSA C22.2#62133-2:2020 Ed. 1 for secondary lithium battery systems. 6507-009-001 Rev AB.3 EN

<60s >300sU.S.A. 5019398 TTaabbllee ooff CCoonntteennttss Warning/Caution/Note Definition ..............................................................................................................................3 Summary of safety precautions ................................................................................................................................3 Introduction ...............................................................................................................................................................7 Product description .................................................................................................................................................7 Indications for use...................................................................................................................................................7 Clinical benefits ......................................................................................................................................................7 Contraindications ....................................................................................................................................................8 Expected service life ...............................................................................................................................................8 Disposal/recycle .....................................................................................................................................................8 Specifications - Power-PRO 2 ..................................................................................................................................8 European REACH - Power-PRO 2 .......................................................................................................................9 China RoHS - Power-PRO 2 .............................................................................................................................10 Standards with required options .............................................................................................................................11 WiFi radio specifications option ..............................................................................................................................11 Specifications - Alvarium .......................................................................................................................................13 European REACH - Alvarium ............................................................................................................................13 China RoHS - Alvarium .....................................................................................................................................14 Product illustration - Power-PRO 2 .........................................................................................................................15 Product illustration - Alvarium.................................................................................................................................16 Contact information ...............................................................................................................................................16 Serial number location - Power-PRO 2 ...................................................................................................................17 Serial number location - Alvarium ...........................................................................................................................17 Setup.......................................................................................................................................................................18 Installation...............................................................................................................................................................19 Installing the cot fastener .......................................................................................................................................19 Installing the in-fastener shut-off.............................................................................................................................19 Selecting the vehicle safety hook ...........................................................................................................................20 Vehicle configuration.............................................................................................................................................21 Positioning of the vehicle safety hook, front to back .................................................................................................22 Positioning of the vehicle safety hook, side to side ...................................................................................................23 Installing the vehicle safety hook ............................................................................................................................24 Operating guidelines...............................................................................................................................................26 Operation ................................................................................................................................................................27 Checking the battery power level............................................................................................................................27 Transferring the patient to the cot ...........................................................................................................................27 Raising or lowering the cot.....................................................................................................................................28 Raising or lowering the cot manually with the manual override..................................................................................29 Applying or releasing a wheel lock or Steer-Lock .....................................................................................................29 Rolling the cot with a patient ..................................................................................................................................30 Pushing or pulling the cot with the transport handle..................................................................................................30 Loading the cot into a vehicle .................................................................................................................................31 Unloading the cot from a vehicle.............................................................................................................................33 Positioning operators and helpers ..........................................................................................................................34 Raising or lowering the backrest.............................................................................................................................35 Raising or lowering the siderails .............................................................................................................................35 Raising or lowering the siderails (XPS option) .........................................................................................................35 Extending or retracting the retractable head section.................................................................................................36 Extending or retracting the retractable foot section ..................................................................................................36 Raising or lowering the footrest ..............................................................................................................................37 Raising or lowering the knee Gatch ........................................................................................................................37 Securing the patient with the restraint straps ...........................................................................................................38 Attaching the shoulder restraints........................................................................................................................39 Attaching the waist restraints.............................................................................................................................40 Attaching the thigh restraints .............................................................................................................................40 Attaching the ankle restraints ............................................................................................................................41 6507-009-001 Rev AB.3 1 EN Adjusting restraint straps .......................................................................................................................................41 Adding a restraint strap extension ..........................................................................................................................42 Securing the child restraint with the X-restraint package...........................................................................................42 Hanging equipment from the equipment hook .........................................................................................................43 Positioning the two-stage IV pole option..................................................................................................................44 Positioning the three-stage IV pole option ...............................................................................................................45 Attaching an oxygen bottle to the oxygen bottle holder option ...................................................................................46 Attaching the base storage net option .....................................................................................................................46 Attaching the backrest storage pouch option ...........................................................................................................47 Attaching the head end storage flat option...............................................................................................................47 Attaching the mattress...........................................................................................................................................47 Inserting the battery ..............................................................................................................................................48 Removing the battery from the product ...................................................................................................................48 Storing the battery.................................................................................................................................................49 Charging the battery..............................................................................................................................................49 Electrical power requirements ................................................................................................................................50 Charger setup.......................................................................................................................................................50 Securing the mounting plate option.........................................................................................................................50 Securing the charger to the mounting plate option ...................................................................................................51 Powering the charger ............................................................................................................................................52 Disconnecting the charger .....................................................................................................................................53 Accessories and parts ............................................................................................................................................54 Cleaning and disinfecting with wipes......................................................................................................................56 Cleaning the product...............................................................................................................................................57 Disinfecting the product ..........................................................................................................................................58 Cleaning the charger ..............................................................................................................................................59 Cleaning the battery ..............................................................................................................................................59 Preventive maintenance .........................................................................................................................................60 Lubrication ...........................................................................................................................................................60 Regular inspection and adjustments .......................................................................................................................60 Every month or two hours .................................................................................................................................60 Every three months or six hours.........................................................................................................................61 Every six months or 12 hours ............................................................................................................................62 Every 12 months or 24 hours.............................................................................................................................62 Wireless notifications ..............................................................................................................................................64 Wireless coexistence notifications ..........................................................................................................................64 EMC information .....................................................................................................................................................65 EN 2 6507-009-001 Rev AB.3 WWaarrnniinngg//CCaauuttiioonn//NNoottee DDeeffiinniittiioonn The words WWAARRNNIINNGG, CCAAUUTTIIOONN, and NNOOTTEE carry special meanings and should be carefully reviewed. WWAARRNNIINNGG Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe potential serious adverse reactions and safety hazards. CCAAUUTTIIOONN Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient or damage to the product or other property. This includes special care necessary for the safe and effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or misuse. NNoottee -- Provides special information to make maintenance easier or important instructions clearer. SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel. WWAARRNNIINNGG Always install the in-fastener shut-off system (if not using a crash-rated cot fastener) in any emergency vehicle that will be used with this cot. Always install the cot fastener by qualified personnel only. Improper installation could result in injury to the patient or operator. Always make sure that all cots meet the installation specifications for the Stryker cot fastener system. Always adjust the rail clamp assembly to match the cot retaining post position for the cot manufacturer and model number. Always position the in-fastener shut-off before you place the cot into service. Do not attempt to operate the cot when loaded into a cot fastener. Always use the in-fastener shut-off to disable the electronic functionality only. Always adjust the mounting location to maintain the proper position of the vehicle safety hook face when you replace an existing vehicle safety hook with a new style. Always have a certified mechanic, familiar with ambulance vehicle construction, install the vehicle safety hook to avoid injury to the patient or operator. Always consult the vehicle manufacturer before vehicle safety hook installation. Make sure that the installation of the vehicle safety hook does not damage or interfere with the brake lines, oxygen lines, fuel lines, fuel tank, or electrical wiring of the vehicle. Do not modify the cot or the vehicle safety hook. If the cot safety bar does not connect with the vehicle safety hook in any of these positions (left, center, or right), modify the vehicle. Always make sure that that the cot safety bar connects with the vehicle safety hook every time before vehicle safety hook installation. Always make sure that the cot safety bar connects with the vehicle safety hook before you remove the cot from the vehicle patient compartment to avoid the risk of injury. Always use screws that are long enough to go through the vehicle patient compartment floor, washer, and nut, with at least two full threads in the nut. The socket head cap screw length depends on the thickness of the vehicle floor. Always operate the cot only when all persons are clear of the mechanisms. Entanglement in powered cot mechanisms can cause serious injury. Always inspect the battery for damage before every use. Do not allow untrained helpers to assist in the operation of the product. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Do not ride on the base of the cot. 6507-009-001 Rev AB.3 3 EN Do not transport the cot sideways to avoid the risk of a cot tip or injury. Always transport the cot in a lowered position, head end or foot end first to minimize the risk of a cot tip or injury. Always keep hands, fingers, and feet away from moving parts. Use caution when you place your hands and feet near the base tubes to raise or lower the cot. Always conduct patient monitoring when the cot is idle. If you hydraulically raise or lower the cot you may temporarily affect electronic patient monitoring equipment. Do not use the product if it has been involved in an accident to avoid the risk of injury due to product damage. Contact Stryker to determine if you need to replace the product. Do not unlock or remove the cot from the cot fastener during vehicle transport. Always center the patient and equipment or accessories. Lock adjustable features and intended lift points before you transport a patient on the product. Always inspect the product for damage if involved in an ambulance accident. Contact Stryker Customer Service or Technical Support for more information. Always use all restraint straps to secure the patient on the product. An unrestrained patient may fall from the product and be injured. Do not leave a patient unattended. Hold the product while a patient is on the product. Do not apply a wheel lock when a patient is on the product or when you move the product to avoid the risk of a cot tip or injury. Always secure the mattress to the product to avoid movement during patient transfer. Do not raise or lower the cot while you are on rough or uneven terrain. Do not replace or apply a wheel lock on a product with worn transport wheels that are less than 6 in. diameter. Always transport the cot at transport height or the lowest possible height to reduce the risk of a cot tip. If possible, obtain additional assistance or take an alternate route. Always avoid high obstacles, such as curbs, steps, or rough terrain to avoid the risk of a cot tip or injury. Always use the specified push/pull locations to reduce the risk of a cot tip or injury. Always stow and latch the transport handle before you load, unload, or use the transport handle to lift the cot. Always support the load of the patient, cot, and accessories after the weight is off of the ground. Always use two operators when a cot is occupied. Do not load the cot into a vehicle with the head section retracted when using a cot fastener. The cot may tip or not connect with the cot fastener. Always make sure that the cot is locked in the cot fastener before you load and unload. Injury may occur if the cot is not secure. Always try to load and unload the cot on level ground to reduce the risk of a cot tip or injury. Do not use the jog function to jog past the set cot load height after the cot safety bar connects with the vehicle safety hook. Do not pull or lift on the cot safety bar when you unload the cot. Do not press the extend (+) button until the safety bar connects with the vehicle safety hook. Always lock the head and foot sections into place before you operate the cot. Do not attach restraint straps to the base tubes, cross tubes, or litter skin. Do not allow the head end storage flat to interfere with the operation of the retractable head section, safety bar, or vehicle safety hook. Do not store items under the mattress. Items under the mattress may interfere with product operation. Do not remove the battery when the product is active. Do not attempt to open the battery pack for any reason, to avoid the risk of electric shock. If the battery pack case is cracked or damaged, do not insert it into the charger. Return damaged battery packs to a service center for recycling. Always avoid direct contact with a wet battery or battery enclosures. Contact may cause injury to the patient or operator. Do not insert a cracked or damaged battery into the charger. Return damaged batteries to a service center for recycling. Do not connect AC and DC power supplies to the battery at the same time to avoid the risk of fire or electric shock. Always have a certified mechanic, familiar with ambulance vehicle construction, secure the mounting plate option and charger. Always make sure that the mounting plate option is secured to the surface before use. Always follow these cleaning and disinfecting guidelines, in addition to your protocols, to maintain hygienic safety. EN 4 6507-009-001 Rev AB.3 Always use any appropriate personal protective equipment while power washing to avoid inhaling contagion. Power washing equipment may aerate contamination. Always wear rubber gloves, in addition to personal protective equipment, when cleaning the battery to reduce the risk of injury. Always disconnect the charger from the wall outlet before cleaning to avoid the risk of electrical hazards. Do not spray fluid directly onto the charger. Do not power wash the charger. Do not use solvents, lubricants, or other chemicals to clean the charger unless otherwise directed. Do not immerse the charger in liquid or allow liquid to collect on top of the charger to avoid the risk of electric shock. Always use only non-conductive materials to wipe the battery. Always avoid excessive water exposure to the battery terminals. Do not directly handle or make contact with the battery terminals while cleaning to avoid the risk of injury. Do not immerse the battery in liquid or allow liquid to collect on top of the battery to avoid the risk of electric shock. Do not use solvents, lubricants, or other chemicals to clean the battery unless otherwise directed. Do not power wash the battery. Do not use bare hands to check for hydraulic leaks. Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be used no closer than 12 inches (30 cm) to any part of PPoowweerr--PPRROO 2, including cables specified by the manufacturer. Avoid stacking or placing other equipment adjacent to PPoowweerr--PPRROO 2 to prevent improper operation of the products. If such use is necessary, carefully observe the cot and the other equipment to verify proper operation. The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation. CCAAUUTTIIOONN Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. Always set the cot load height before you place the cot into service. Always clear any obstacles that may interfere and cause injury to the operator or patient before operating the product. Do not use siderails as a patient restraint device. Always set the transport wheels safely on the ground when you unload the cot from the vehicle patient compartment to avoid the risk of product damage. Do not use siderails as a push/pull device or to steer the product. Do not sit or stand on the siderails (XPS option). Do not use the siderails (XPS option) as a patient transfer device or surface (for example, to slide a patient from the cot to another surface). Do not position patients with full weight on the siderails (XPS option). Do not use the siderails as a push/pull device or to steer the product. Do not entangle the restraint straps in the base frame when you raise or lower the cot. Do not load the equipment hook above the safe working load of 35 lb (15.8 kg). Always remove all accessories or equipment from the equipment hook when in the vehicle. Do not load the IV pole above the safe working load of 25 lb (11.3 kg). Do not load the oxygen bottle holder above the safe working load of 15 lb (6.8 kg). Do not use two oxygen bottle holders at the same time. Do not load the base storage net above the safe working load of 20 lb (9 kg). Always be careful when you retract the base to avoid damaging items that are stored in the base storage net. Do not load the single-sided backrest storage pouch above the safe working load of 10 lb (4.5 kg). Do not load the dual-sided backrest storage pouch above the safe working load of 20 lb (9 kg). Do not allow the storage pouch to interfere with the operation of the retractable head section. Do not load the head end storage flat above the safe working load of 40 lb (18 kg). Always remove the battery if you do not intend to use the product for more than 24 hours or longer. 6507-009-001 Rev AB.3 5 EN Always place the electrical charger power cord where it will not be stepped on, tripped over, or otherwise subjected to damage or stress. Do not touch the battery receptacle terminals with metal objects. Always grasp and pull the plug, not the cord, when you disconnect the charger to avoid the risk of damage to the electrical plug and cord. Always remove the battery before you wash the product. Do not clean, service, or perform maintenance while the product is in use. Do not steam clean or ultrasonically clean the product. Do not exceed 180 F (82 C) as the maximum water temperature. Do not exceed 1500 psi (130.5 bar) as the maximum water pressure. If you are using a hand held wand to wash the product, keep the pressure nozzle at a minimum of 24 in. (61 cm) from the product. Always use authorized parts to avoid the risk of product damage. Do not lubricate the bearings in the X-frame as it will degrade the performance of the cot and may void its warranty. Changes or modifications to the AAllvvaarriiuumm Battery Management System, not expressly approved by Stryker, could void the user's authority to operate the equipment. EN 6 6507-009-001 Rev AB.3 IInnttrroodduuccttiioonn This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance of this product. CCAAUUTTIIOONN Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. NNoottee This manual is a permanent part of the product and should remain with the product even if the product is sold. Stryker continually seeks advancements in product design and quality. This manual contains the most current product information available at the time of printing. There may be minor discrepancies between your product and this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770. PPrroodduucctt ddeessccrriippttiioonn The Stryker PPoowweerr--PPRROO 2 is a powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). The AAllvvaarriiuumm rechargeable battery powers the hydraulic lift system and allows operators to raise and lower the cot using the powered controls on the foot end lift bars. The cot features low transport height capability. The cot has an adjustable load height feature to allow the cot to be set to different ambulance deck heights during loading and unloading. The cot is equipped with a manual back-up release handle to allow the operation of cot functions in the event of power loss. Foot end LED lights illuminate transport areas and reflective markings aid in cot visibility. The cot is also equipped with the following: a retractable head section for 360 degree mobility in any height position, siderails, adjustable backrest, patient restraint straps, and standard mechanical steer and wheel locks. The cot can be equipped various optional accessories that assist with the transport of the patient. The cot litter can be articulated in multiple positions. The cot service interface allows service technicians to acquire cot data and update software. PPoowweerr--PPRROO 2 is compatible with, and can be inductively charged by, the Stryker PPoowweerr--LLOOAADD and PPeerrffoorrmmaannccee--

LLOOAADD fastening systems. PPoowweerr--PPRROO 2 is also compatible with mass casualty, wall mount, and floor mount fasteners. AAllvvaarriiuumm Battery Management System is comprised of a lithium iron phosphate battery pack and a universal charger. The rechargeable battery acts as a power source for the PPoowweerr--PPRROO 2 cot. IInnddiiccaattiioonnss ffoorr uussee PPoowweerr--PPRROO 2 is intended to transport a patient to or from an emergency or non-emergency location, primarily within an emergency transport vehicle, to a healthcare facility. PPoowweerr--PPRROO 2 is intended for adult, adolescent, and child occupants who can be effectively secured by patient restraint straps on the product. Intended operators include trained professionals

(emergency medical services and medical care center personnel) and medical first responders. PPoowweerr--PPRROO 2 is not intended for extended stay, use as a hospital bed, or devices that modify air pressure, such as hyperbaric chambers. CClliinniiccaall bbeenneeffiittss Cot: patient transport Fastener: support cot for transport 6507-009-001 Rev AB.3 7 EN Cot and fastener system: support and transport patients CCoonnttrraaiinnddiiccaattiioonnss None known. EExxppeecctteedd sseerrvviiccee lliiffee PPoowweerr--PPRROO 2 has a 7 year expected service life under normal use conditions and with appropriate periodic maintenance. AAllvvaarriiuumm charger has a 7 year expected service life under normal use conditions. AAllvvaarriiuumm battery has a 2 year expected service life under normal use conditions. DDiissppoossaall//rreeccyyccllee Always follow the current local recommendations and/or regulations governing environmental protection and the risks associated with recycling or disposing of the equipment at the end of its useful life. SSppeecciiffiiccaattiioonnss -- PPoowweerr--PPRROO 22 NNoottee -- Safe working load indicates the sum of the patient, mattress, and accessory weight. Extended Mid Retracted Backrest articulation Length Overall width Height1 Weight2 Caster diameter/width Minimum operators required for loading/unloading an occupied cot Minimum operators required for loading/unloading an unoccupied cot Recommended fastener systems 700 lb 318 kg 0 to 75 84 in. 81 in. 60 in. 22.6 in 213.4 cm 205.7 cm 152.4 cm 57.4 cm Adjustable from 14.4 in. to 41 in. Adjustable from 36.6 cm to 104 cm 59 kg 15 cm/5 cm 130 lb 6 in./2 in. 2 1 Model 6390 PPoowweerr--LLOOAADD, Model 6392 PPeerrffoorrmmaannccee--

LLOOAADD, Model 6370 or 6377 floor mount, Model 6371 wall mount Recommended loading height Up to 36 in. Recommended transport height (excluding mattress) 25 in. Up to 91 cm 63.5 cm Hydraulic oil PPeennttoossiinn CFH 11S EN 8 6507-009-001 Rev AB.3 Power system Battery (650700080301) Charger (650700450301) Cot duty cycle Standards 25.6 VDC LiFePO4 100-240 VAC, 50/60 Hz, 1A 12-34 VDC, 5A 16.7%

ANSI/AAMI ES 60601-1, 60601-1-12, 60601-1-2, BS EN 1865-2, BS EN 1865-3, AS/NZS-4535, SAE J3027, BS EN-

1789, BS EN 597-1, 16 CFR 1632 For standards that require specific options, see Standards withrequiredoptions (page 11). 1 Height is measured from bottom of mattress at seat section to ground level. 2 Cot is weighed with one battery and without mattress and restraints. Stryker reserves the right to change specifications without notice. The yellow and black color scheme is a proprietary trademark of Stryker Corporation. Labels may be unreadable from a viewing distance greater than 12 inches. PPoowweerr--PPRROO 2 is designed to conform to:

NFPA-1917 CAAS-GVS KKK-A-1822 EEnnvviirroonnmmeennttaall ccoonnddiittiioonn OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn Temperature Relative humidity Atmospheric pressure EEuurrooppeeaann RREEAACCHH -- PPoowweerr--PPRROO 22 In accordance with the European REACH regulation and other environmental regulatory requirements, the components that contain declarable substances are listed. DDeessccrriippttiioonn NNuummbbeerr Base controller PCBA assembly 650700080800 Caster nut Cot comm board 6090-001-009 650700080203 Foot end interface board PCBA 650700080810 SSuubbssttaannccee ooff vveerryy hhiigghh ccoonncceerrnn

((SSVVHHCC)) cchheemmiiccaall nnaammee Lead, lead monoxide (lead oxide), diboron trioxide Lead Octamethylcyclotetrasiloxane (D4) Lead, lead monoxide (lead oxide), diboron trioxide 6507-009-001 Rev AB.3 9 EN 130 F(54 C)-30 F (-34 C)130 F(54 C)-30 F (-34 C)93%10%93%10%1060 hPa6201060 hPa500 DDeessccrriippttiioonn Gas spring yoke Gas spring yoke end NNuummbbeerr 650700080178 650700080179 Lift motor cable assembly 650700080868 Light module cable assembly 650700080890 Mattress, knee Gatch bolster 6500-002-150 Mattress, knee Gatch bolster, grey 6506-002-150 Mattress, knee Gatch bolster, XPS 6500-003-130 Mattress, knee Gatch bolster, grey 6506-003-130 NFMIC - shielded PCBA assembly 650700080830 WiFi module HBC assembly 650700080202 650700080800 CChhiinnaa RRooHHSS -- PPoowweerr--PPRROO 22 SSuubbssttaannccee ooff vveerryy hhiigghh ccoonncceerrnn

((SSVVHHCC)) cchheemmiiccaall nnaammee Lead Lead Lead Lead

(2H-benzotriazol2-yl)-4, 6-di-tert-

pentylphenol

(2H-benzotriazol2-yl)-4, 6-di-tert-

pentylphenol

(2H-benzotriazol2-yl)-4, 6-di-tert-

pentylphenol

(2H-benzotriazol2-yl)-4, 6-di-tert-

pentylphenol Lead, lead monoxide (lead oxide), diboron trioxide Diboron trioxide Lead, lead monoxide (lead oxide), diboron trioxide, 2-methyl-1-(4-

methylthiophenyl)-2-morpholinopropan-

1-one HHaazzaarrddoouuss ssuubbssttaanncceess LLeeaadd ((PPbb)) MMeerrccuurryy

((HHgg)) CCaaddmmiiuumm

((CCdd)) HHeexxaavvaalleenntt cchhrroommiiuumm

((CCrr ((VVll)))) PPoollyybbrroommii--

nnaatteedd bbiipphheennyyllss

((PPBBBB)) PPoollyybbrroommii--

nnaatteedd ddiipphheennyyll eetthheerrss

((PPBBDDEE)) O O O O O DDeessccrriipp--

ttiioonn NNuummbbeerr Actuator assembly 650700020-

026 650700080-

810 Foot end interface board PCBA Gateway 4.0 PCBA 521206000-

900 650700080-

202 650700080-

800 650700020-

198 O Cot WiFi module Base controller PCBA assembly MTS sensor assembly EN 10 X X X X X X X X X X X X X X X X X X X X X X X X X X X X X X 6507-009-001 Rev AB.3 HHaazzaarrddoouuss ssuubbssttaanncceess LLeeaadd ((PPbb)) MMeerrccuurryy

((HHgg)) CCaaddmmiiuumm

((CCdd)) HHeexxaavvaalleenntt cchhrroommiiuumm

((CCrr ((VVll)))) PPoollyybbrroommii--

nnaatteedd bbiipphheennyyllss

((PPBBBB)) PPoollyybbrroommii--

nnaatteedd ddiipphheennyyll eetthheerrss

((PPBBDDEE)) X X X X X X X X X X X X X X X X X X X X DDeessccrriipp--

ttiioonn NNuummbbeerr Cot caster nut 6090-001-

009 O O 650700080-

890 650700080-

891 O 650700080-

892 O Light module cable assembly User interface bottom cable assembly User interface top cable assembly This table is prepared in accordance with the provisions of SJ/T 11364. O: Indicates that said hazardous substance contained in all of the homogenous materials used for this part is below the limit requirement of GB/T 26572. X: Indicates that said hazardous substance contained in at least one of the homogenous materials used for this part is above the limit requirement of GB/T 26572. Enterprises may further provide in this box technical explanation for marking X based on their actual circumstances. SSttaannddaarrddss wwiitthh rreeqquuiirreedd ooppttiioonnss To be compliant with the standards, you must use the following required options on your cot. OOppttiioonn sseelleeccttiioonn CCrraasshh--tteesstt ssttaannddaarrdd RReessttrraaiinntt ppaacckkaaggee FFaasstteenneerr SAE J3027 BS EN 1789 X-restraint package (6500-001-430) X-restraint package (6500-001-430) PPeerrffoorrmmaannccee--LLOOAADD and PPoowweerr--

LLOOAADD PPeerrffoorrmmaannccee--LLOOAADD and PPoowweerr--

LLOOAADD WWiiFFii rraaddiioo ssppeecciiffiiccaattiioonnss ooppttiioonn Manufacturer/model Chipset IEEE 802.11 RF bands Silex SX-SDMAC-2832S+

Qualcomm Atheros QCA9377-3 a/b/g/n/ac 2.4 GHz, 5 GHz 6507-009-001 Rev AB.3 11 EN Encryption Authentication 802.1X Client certificates Supported data rates Hash function compatibility Channel plan Other IItteemm Operating frequencies Frequency steps AES and TKIP

(TKIP is not supported with WPA2) WPA Personal/Enterprise and WPA2 Personal/Enterprise PEAP-MSCHAP - v2 Cannot accept or upload certificates 802.11b/g: 1-54 Mbps 802.11a: 6-54 Mbps 802.11n: MCS0-7 802.11ac: MCS0-9 (compatible) SHA-1 and SHA-2 server side certificate recognition for PEAP-MSCHAP - v2 2.4 GHz: All channels supported 5 GHz: All channels supported

(Recommend against the use of DFS and ISM channels) Leverage hospital SSID Support for 802.11r Support for Cisco CCX (Fast roaming) SSppeecciiffiiccaattiioonn -- CChhiippsseett QQCCAA99337777--33 ((QQuuaallccoommmm AAtthheerrooss)) BBaanndd 2.4GHz 5GHz 2.4GHz 5GHz Not applicable MMooddee 11b 11g/n/ac 11g/n/ac 11a/n/ac 11n/ac 11ac 11b/g/n 11a/n/ac 11n/ac 11ac 11b MMiinn 2412 2412 2422 5180 5190 5210 MMaaxx 2472 2472 2462 5825 5795 5775 5 20 40 80 UUnniitt MHz MHz MHz MHz MHz MHz MHz MHz MHz MHz DSSS (DBPSK, DQPSK, CCK) Not applicable OFDM (BPSK, QPSK, 16QAM, 64QAM) OFDM (BPSK, QPSK, 16QAM, 64QAM, 255QAM) Not applicable Not applicable Modulation types Not applicable 11a/g/n Not applicable 11ac Maximum ERP Not applicable Not applicable

-8.648/21.352 dBW/dBm EN 12 6507-009-001 Rev AB.3 SSppeecciiffiiccaattiioonnss -- AAllvvaarriiuumm CChhaarrggeerr ((665500770000445500330011)) BBaatttteerryy ((665500770000008800330011)) Electrical input 12-34 VDC, 5A Electrical output Not applicable Not applicable 25.6 VDC LiFePO4 Height Width Length Weight 6.09 in. 4.46 in. 7.79 in. 1.55 lb 154.69 mm 113.28 mm 197.87 mm 0.70 kg Enclosure protection Not applicable 3.62 in. 3.18 in. 6.05 in. 2.15 lb IP36 91.95 mm 80.77 mm 153.67 mm 0.98 kg Standards IEC 62368 IEC 62133-2, IEC 60529: IP36, SAE J3043 EEnnvviirroonnmmeennttaall ccoonnddiittiioonn OOppeerraattiioonn CChhaarrggiinngg SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn Temperature Relative humidity Atmospheric pressure Specifications are approximate and may vary from product to product or as a result of power supply fluctuations. Hereby, Stryker declares that the radio equipment type short range device is in compliance with Directive 2014/53/EU. The full text of the EU declaration of conformity is available at the following internet address: http://techweb.stryker.com/EMS/

EU%20Declaration%20of%20Conformity/index.html. EEuurrooppeeaann RREEAACCHH -- AAllvvaarriiuumm In accordance with the European REACH regulation and other environmental regulatory requirements, the components that contain declarable substances are listed. DDeessccrriippttiioonn NNuummbbeerr SSuubbssttaannccee ooff vveerryy hhiigghh ccoonncceerrnn

((SSVVHHCC)) cchheemmiiccaall nnaammee Battery charger PCBA 650700080820 Lead, diboron trioxide 12 VDC cable, automotive 6500-201-247 Lead, fatty acids, C16-18, lead salts 6507-009-001 Rev AB.3 13 EN 104 F(40 C)32 F (0 C)104 F(40 C)50F (10 C)140 F(60 C)-4 F (-20 C)75%30%75%30%75%10%1060 hPa7001060 hPa7001060 hPa500 CChhiinnaa RRooHHSS -- AAllvvaarriiuumm DDeessccrriipp--

ttiioonn NNuummbbeerr HHaazzaarrddoouuss ssuubbssttaanncceess LLeeaadd ((PPbb)) MMeerrccuurryy

((HHgg)) CCaaddmmiiuumm

((CCdd)) HHeexxaavvaalleenntt cchhrroommiiuumm

((CCrr ((VVll)))) PPoollyybbrroommii--

nnaatteedd bbiipphheennyyllss

((PPBBBB)) PPoollyybbrroommii--

nnaatteedd ddiipphheennyyll eetthheerrss

((PPBBDDEE)) Battery charger PCBA 650700080-

820 O X X X X X This table is prepared in accordance with the provisions of SJ/T 11364. O: Indicates that said hazardous substance contained in all of the homogenous materials used for this part is below the limit requirement of GB/T 26572. X: Indicates that said hazardous substance contained in at least one of the homogenous materials used for this part is above the limit requirement of GB/T 26572. Enterprises may further provide in this box technical explanation for marking X based on their actual circumstances. EN 14 6507-009-001 Rev AB.3 PPrroodduucctt iilllluussttrraattiioonn -- PPoowweerr--PPRROO 22 FFiigguurree 11 PPoowweerr--PPRROO 22 A B C D E F G H I J Foot end light Foot section release lever Retractable foot section Manual back-up release handle Battery Cot control switch Transport handle Footrest Red lifting loop XPS siderail K L M N O P Q R S T Backrest Backrest adjustment handle Retractable head section Head section release handle Safety bar Load wheel Wheel lock/SStteeeerr--LLoocckk Transport wheel Cot retaining post Height sensor housing 6507-009-001 Rev AB.3 15 EN CDEFGHIKLMNJAOPBDQRST PPrroodduucctt iilllluussttrraattiioonn -- AAllvvaarriiuumm A B C D E F FFiigguurree 22 AAllvvaarriiuumm Battery Battery indicator button Charger Battery release button AC power cord DC power cord CCoonnttaacctt iinnffoorrmmaattiioonn Contact Stryker Customer Service or Technical Support at: 1-800-327-0770. Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA NNoottee -- The user and/or the patient should report any serious product-related incident to both the manufacturer and the Competent authority of the European Member State where the user and/or patient is established. To view your operations or maintenance manual online, see https://techweb.stryker.com/. Have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical Support. Include the serial number in all written communication. EN 16 6507-009-001 Rev AB.3 CABDEF SSeerriiaall nnuummbbeerr llooccaattiioonn -- PPoowweerr--PPRROO 22 See below for the cot (A) serial number location. SSeerriiaall nnuummbbeerr llooccaattiioonn -- AAllvvaarriiuumm See below for the battery (B) and charger (C) serial number locations. 6507-009-001 Rev AB.3 17 EN ABC SSeettuupp During setup, unpack the cartons and check all items for proper operation. Confirm proper operation before you place the product into service. WWAARRNNIINNGG -- Always install the in-fastener shut-off system (if not using a crash-rated cot fastener) in any emergency vehicle that will be used with this cot. Remove all the shipping and packaging materials from the product before use. Remove the cotter pin from the manual release bracket so you can extend the cot base frame. The vehicle patient compartment where the product will be used must have a:

Smooth rear edge for loading Level floor large enough for the folded product Stryker cot fastener system Space to install the vehicle safety hook In fastener shut-off module installed, if using an antler style cot fastener NNoottee -- Loose items or debris on the vehicle patient compartment floor can interfere with the operation of the vehicle safety hook and product fastener. Keep the vehicle patient compartment floor clear. Unpack the battery and charger. Fully charge the battery before use. Check the power cords, cables, and optional mounting brackets for any damage. When necessary, modify the vehicle to fit the cot. Do not modify the cot. EN 18 6507-009-001 Rev AB.3 IInnssttaallllaattiioonn IInnssttaalllliinngg tthhee ccoott ffaasstteenneerr The Stryker cot fastener systems are compatible only with cots that conform to the installation specifications. WWAARRNNIINNGG Always install the cot fastener by qualified personnel only. Improper installation could result in injury to the patient or operator. Always make sure that all cots meet the installation specifications for the Stryker cot fastener system. Always adjust the rail clamp assembly to match the cot retaining post position for the cot manufacturer and model number. These instructions are intended for cots with antler style cot fastener systems. For crash-rated cot fasteners, see the appropriate Operations Manual for installation instructions. IInnssttaalllliinngg tthhee iinn--ffaasstteenneerr sshhuutt--ooffff These instructions are intended for cots with antler style cot fastener systems. For crash-rated cot fasteners, see the appropriate Operations Manual for installation instructions. WWAARRNNIINNGG Always position the in-fastener shut-off before you place the cot into service. Do not attempt to operate the cot when loaded into a cot fastener. Always use the in-fastener shut-off to disable the electronic functionality only. Always install the in-fastener shut-off system (if not using a crash-rated cot fastener) in any emergency vehicle that will be used with this cot. The cot and antler style cot fastener system have an integrated in-fastener shut-off function that disables the cot motor when you secure the cot into the cot fastener. Tighten the bolts to secure the fastener before you install the shut-off bracket. Install the shut-off bracket onto the rail clamp assembly before you place the cot into service. 1. Raise the base and push the cot into the vehicle patient compartment. Follow appropriate loading instructions. 2. Secure the extended head section of the cot into the cot fastener antler. 3. Secure the cot post into the fastener rail clamp. 4. Adjust the shut-off bracket along the rail clamp until the diamond (A) on the outer rail label is centered between the pop rivet heads (B) on the in-ambulance shut-off (Figure 3). 5. Using a T27 Torx driver, securely fasten the bolts to attach the shut-off bracket to the rail clamp assembly. 6. Press the retract (-) button to check that the motor does not turn on while the cot is in the fastener. The cot battery LED indicator will still illuminate. If the motor turns on, readjust the shut-off bracket. 6507-009-001 Rev AB.3 19 EN SSeelleeccttiinngg tthhee vveehhiiccllee ssaaffeettyy hhooookk FFiigguurree 33 AAddjjuusstt tthhee sshhuutt--ooffff bbrraacckkeett The vehicle safety hook is a device that ships with the cot. The cot safety bar and vehicle safety hook keep the cot from being accidentally removed from the vehicle and provide increased operator assurance and confidence when loading and unloading. WWAARRNNIINNGG -- Always adjust the mounting location to maintain the proper position of the vehicle safety hook face when you replace an existing vehicle safety hook with a new style. NNoottee -- These instructions are intended for cots with antler style cot fastener systems. For crash-rated cot fasteners, see the appropriate Operations Manual for installation instructions. Crash-rated cot fasteners are shipped and installed with a vehicle safety hook, so no additional hook is needed. The vehicle safety hook was designed for compatibility and proper operation when loading and unloading the cot from a vehicle that is compliant with Federal Regulation KKK-A-1822. Stryker offers three different types of vehicle safety hooks that are ordered and shipped with your cot. These vehicle safety hook types meet the needs of various emergency vehicle configurations, specifically the length and location of the floor structure support that is located in the rear of the vehicle. To select which vehicle safety hook is appropriate for your vehicle configuration:

Consider the location of the floor structure support where there is adequate room to mount the vehicle safety hook. Mount the vehicle safety hook into the back of the vehicle. Provide bumper clearance to allow the operators to load and unload the cot from the vehicle. Note the differences in vehicle design. Each vehicle safety hook provides a different mounting location option to maintain the appropriate distance between the face of the vehicle safety hook and the edge of the door sill. Due to the differences in vehicle dimensions and the floor structure support locations, each vehicle safety hook allows for a different mounting location. Select the correct position for your vehicle safety hook installation. Positioningofthevehiclesafetyhook,fronttoback (page 22) Positioningofthevehiclesafetyhook,sidetoside (page 23) EN 20 6507-009-001 Rev AB.3 AB VVeehhiiccllee ccoonnffiigguurraattiioonn FFiigguurree 44 VVeehhiiccllee ssaaffeettyy hhooookk ttyyppeess WWAARRNNIINNGG Always have a certified mechanic, familiar with ambulance vehicle construction, install the vehicle safety hook to avoid injury to the patient or operator. Always consult the vehicle manufacturer before vehicle safety hook installation. Make sure that the installation of the vehicle safety hook does not damage or interfere with the brake lines, oxygen lines, fuel lines, fuel tank, or electrical wiring of the vehicle. CCAAUUTTIIOONN -- Always set the cot load height before you place the cot into service. The cot is compatible with all vehicle deck heights that meet the Federal Specification for the Star-of-Life Ambulance KKK-

A-1822. See specifications for maximum load height. According to Federal Specification for the Star-of-Life Ambulance KKK-A-1822:

The rear of the ambulance shall be furnished with a sturdy, full-width, rear bumper, with step secured to the vehicles chassis frame. The tread of the step shall have a minimum depth of 5 in. (13 cm) and a maximum depth of 10 in. (25 cm). If the step protrudes more than 7 in. (18 cm) from the rear of the vehicle, a fold-up step shall be furnished. According to federal regulations (reference KKK-A-1822), the bumper height of the vehicle shall be installed equidistant 2 in. ( 5 cm) from the vehicle floor to the ground level, which is defined as the vehicle deck height. Installation of the vehicle safety hook into any vehicle compliant with this federal specification provides adequate clearance for the cot base to lower to its fully extended position. 6507-009-001 Rev AB.3 21 EN 6060-036-0186092-036-0186060-036-017 A B C D E F FFiigguurree 55 DDeecckk aanndd bbuummppeerr hheeiigghhtt Deck height (DH) Bumper height Vehicle safety hook Sill edge Sill Bumper depth PPoossiittiioonniinngg ooff tthhee vveehhiiccllee ssaaffeettyy hhooookk,, ffrroonntt ttoo bbaacckk Before vehicle safety hook installation, check the front to back and side to side positioning when you unload and load the cot. To check the front to back positioning:

1. Select the appropriate vehicle safety hook (Selectingthevehiclesafetyhook (page 20)). 2. Position the vehicle safety hook at least 3-3/4 in. from the leading edge of the door sill (A). The recommended distance from the face of the safety hook to be no less than 3-3/4 in. 3. Check that you can secure the vehicle safety hook to the mount in the back of the vehicle. 4. Check that you have adequate bumper clearance to allow the cot to be loaded and unloaded from the vehicle. 5. Confirm the side to side placement of the vehicle safety hook (Positioningofthevehiclesafetyhook,sidetoside (page 23)). EN 22 6507-009-001 Rev AB.3 DH22ABCDEFAB A B FFiigguurree 66 VVeehhiiccllee ssaaffeettyy hhooookk ppllaacceemmeenntt Sill Floor structure support PPoossiittiioonniinngg ooff tthhee vveehhiiccllee ssaaffeettyy hhooookk,, ssiiddee ttoo ssiiddee Before vehicle safety hook installation, check the front to back and side to side positioning when you unload and load the cot. WWAARRNNIINNGG Do not modify the cot or the vehicle safety hook. If the cot safety bar does not connect with the vehicle safety hook in any of these positions (left, center, or right), modify the vehicle. Always make sure that that the cot safety bar connects with the vehicle safety hook every time before vehicle safety hook installation. To check the side to side positioning:

1. Remove the cot from the cot fastener and unload it from the vehicle. NNoottee -- Note the position of the cot load wheels and the cot safety bar when you remove the cot. 2. Mark the center of the cot safety bar on the vehicle floor. 3. Check that the position marked in step 3 is where the cot safety bar connects with the vehicle safety hook every time when you unload the cot in a variety of positions (such as all the way to the left and all the way to the right). 6507-009-001 Rev AB.3 23 EN 6060-036-0186060-036-0176092-036-018AB IInnssttaalllliinngg tthhee vveehhiiccllee ssaaffeettyy hhooookk Before vehicle safety hook installation, the certified mechanic should plan for the placement of the vehicle safety hook in the rear of the vehicle patient compartment. WWAARRNNIINNGG Always have a certified mechanic, familiar with ambulance vehicle construction, install the vehicle safety hook to avoid injury to the patient or operator. Always consult the vehicle manufacturer before vehicle safety hook installation. Make sure that the installation of the vehicle safety hook does not damage or interfere with the brake lines, oxygen lines, fuel lines, fuel tank, or electrical wiring of the vehicle. Always make sure that the cot safety bar connects with the vehicle safety hook before you remove the cot from the vehicle patient compartment to avoid the risk of injury. Always use screws that are long enough to go through the vehicle patient compartment floor, washer, and nut, with at least two full threads in the nut. The socket head cap screw length depends on the thickness of the vehicle floor. HHaarrddwwaarree rreeqquuiirreedd ((nnoott ssuupppplliieedd))::

(2) Grade 5, minimum 1/4-20 socket head cap screws * for the short vehicle safety hook or long vehicle safety hook

(2) Grade 5, minimum 1/4-20 flat socket head cap screws * for the J vehicle safety hook

(2) Flat washers

(2) Lock washers

(2) 1/4-20 nuts 1. Determine the correct vehicle safety hook front to back and side to side positioning, so the cot safety bar connects to the vehicle safety hook every time. Positioningofthevehiclesafetyhook,fronttoback (page 22) Positioningofthevehiclesafetyhook,sidetoside (page 23) 2. Drill the holes for the screws. 3. Fasten the vehicle safety hook to the vehicle patient compartment floor. 4. Check that the cot safety bar connects with the vehicle safety hook before you remove the cot from the vehicle patient compartment. EN 24 6507-009-001 Rev AB.3 FFiigguurree 77 SSaaffeettyy bbaarr sseeccuurreedd iinn tthhee vveehhiiccllee ssaaffeettyy hhooookk A B C D E FFiigguurree 88 VVeehhiiccllee ssaaffeettyy hhooookk ppllaacceemmeenntt Top view of vehicle Vehicle safety hook Squad bench Bumper Door frame After installation, check that the cot legs lock into the load position without contacting the vehicle bumper. 6507-009-001 Rev AB.3 25 EN ABCDE OOppeerraattiinngg gguuiiddeelliinneess WWAARRNNIINNGG Always operate the cot only when all persons are clear of the mechanisms. Entanglement in powered cot mechanisms can cause serious injury. Always inspect the battery for damage before every use. Do not allow untrained helpers to assist in the operation of the product. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Do not ride on the base of the cot. Do not transport the cot sideways to avoid the risk of a cot tip or injury. Always transport the cot in a lowered position, head end or foot end first to minimize the risk of a cot tip or injury. Always keep hands, fingers, and feet away from moving parts. Use caution when you place your hands and feet near the base tubes to raise or lower the cot. Always install the in-fastener shut-off system (if not using a crash-rated cot fastener) in any emergency vehicle that will be used with this cot. Always conduct patient monitoring when the cot is idle. If you hydraulically raise or lower the cot you may temporarily affect electronic patient monitoring equipment. Do not use the product if it has been involved in an accident to avoid the risk of injury due to product damage. Contact Stryker to determine if you need to replace the product. Do not unlock or remove the cot from the cot fastener during vehicle transport. Always center the patient and equipment or accessories. Lock adjustable features and intended lift points before you transport a patient on the product. Do not attempt to operate the cot when loaded into a cot fastener. Always inspect the product for damage if involved in an ambulance accident. Contact Stryker Customer Service or Technical Support for more information. CCAAUUTTIIOONN -- Always clear any obstacles that may interfere and cause injury to the operator or patient before operating the product. Operate the product only as described in this manual. Read all labels and instructions on the product before use. Practice changing height positions and loading the cot until you fully understand the operation of the product. EN 26 6507-009-001 Rev AB.3 OOppeerraattiioonn CChheecckkiinngg tthhee bbaatttteerryy ppoowweerr lleevveell A charged battery, in working condition, provides at least 14 lifts with a 250 lb (113.4 kg) patient (actual results may vary). The charger LED indicator bars show the battery power level. SSttaattuuss Discharging Low battery Charging Error FFiigguurree 99 BBaatttteerryy ppoowweerr lleevveell BBaatttteerryy LLEEDD iinnddiiccaattoorr Four LED bars = 76-100% charge Three LED bars = 51-75% charge Two LED bars = 26-50% charge One LED bar = 15-25% charge

<15% charge One LED blinks five times, repeated two to three times LED indicating current charge percentage is blinking Press LED indicator button and outermost LEDs blink five times, repeated three times See Troubleshooting in the Maintenance Manual NNoottee Use only Stryker approved batteries. Lock the cot into the powered cot fastener to automatically charge the battery. There are no cables or connectors required to charge. TTrraannssffeerrrriinngg tthhee ppaattiieenntt ttoo tthhee ccoott WWAARRNNIINNGG Always use all restraint straps to secure the patient on the product. An unrestrained patient may fall from the product and be injured. 6507-009-001 Rev AB.3 27 EN Do not leave a patient unattended. Hold the product while a patient is on the product. Do not apply a wheel lock when a patient is on the product or when you move the product to avoid the risk of a cot tip or injury. Always secure the mattress to the product to avoid movement during patient transfer. CCAAUUTTIIOONN -- Do not use siderails as a patient restraint device. To transfer the patient to the cot:

1. Roll the cot to the patient (Rollingthecotwithapatient (page 30)). 2. Place the cot beside the patient. Raise or lower the cot to the level of the patient. 3. Lower the siderails and open the restraint straps. 4. Transfer the patient to the cot. Follow accepted EMS procedures. 5. Secure the patient to the cot with all of the restraint straps. 6. Raise the siderails and adjust the backrest and footrest as necessary. RRaaiissiinngg oorr lloowweerriinngg tthhee ccoott You can raise or lower an unoccupied cot with one operator. If a patient is on the cot, a minimum of two trained operators are required to raise or lower the cot (one located at each end of the cot). WWAARRNNIINNGG Always keep hands, fingers, and feet away from moving parts. Use caution when you place your hands and feet near the base tubes to raise or lower the cot. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Do not raise or lower the cot while you are on rough or uneven terrain. There are two identical cot control switches located on your PPoowweerr--PPRROO 2 cot. Press the button on either of these switches to raise (extend) the cot, lower (retract) the cot, or release the cot from PPoowweerr--LLOOAADD, if applicable (Figure 10). RReeffeerreennccee A B C EN 28 FFiigguurree 1100 CCoott ccoonnttrrooll sswwiittcchheess NNaammee Foot end light Indicator light Retract (-) DDeessccrriippttiioonn Press to turn the foot end light on or off Illuminates when you reach transport height (see item D) Press and hold to lower the litter or retract the cot undercarriage 6507-009-001 Rev AB.3 CDABE RReeffeerreennccee NNaammee DDeessccrriippttiioonn D E Release or transport height Extend (+) Press to unlock the cot (this function operates only when within range of a PPoowweerr--LLOOAADD cot fastener) Press to raise or lower the cot to transport height NNoottee -- The cot will stop moving when you reach transport height. Press and hold to raise the litter or extend the cot undercarriage RRaaiissiinngg oorr lloowweerriinngg tthhee ccoott mmaannuuaallllyy wwiitthh tthhee mmaannuuaall oovveerrrriiddee In the event of loss of electrical function, you can use the cot manual override. This allows manual operation of the cot until the restoration of the electrical, powered functions. Use the red manual back-up release handle to raise or lower the cot. WWAARRNNIINNGG Always keep hands, fingers, and feet away from moving parts. Use caution when you place your hands and feet near the base tubes to raise or lower the cot. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Do not raise or lower the cot while you are on rough or uneven terrain. The manual back-up release handle is located along the patient right side of the lower lift bar at the foot end of the cot. To raise or lower the cot with the manual back-up release handle:

1. Both operators: Lift the cot during the raise or lower operation to support the weight of the cot at each end. 2. Operator 1 (foot end):

a. Pull the manual back-up release handle toward the lift bar. b. While you pull the manual back-up release handle, raise or lower the cot to the desired position. c. Release the handle to lock the cot into position. NNoottee -- Both operators must lift the cot weight off of the transport wheels to use the manual extend or retract while a patient is on the cot. AAppppllyyiinngg oorr rreelleeaassiinngg aa wwhheeeell lloocckk oorr SStteeeerr--LLoocckk WWAARRNNIINNGG Do not apply a wheel lock when a patient is on the product or when you move the product to avoid the risk of a cot tip or injury. Do not replace or apply a wheel lock on a product with worn transport wheels that are less than 6 in. diameter. Do not leave a patient unattended. Hold the product while a patient is on the product. NNoottee -- Wheel locks help prevent the product from rolling while unattended. Wheel locks may not provide sufficient resistance on all surfaces or under loads. To apply a wheel lock (A), press the red pedal down and away from the middle of the cot X-frame (Figure 11). To apply SStteeeerr--LLoocckk (B), press the red pedal down and toward the middle of the cot X-frame (Figure 12). 6507-009-001 Rev AB.3 29 EN To release a wheel lock or SStteeeerr--LLoocckk (C), press down on the top of the pedal with your foot or lift up on the pedal with your toe. The top of the pedal will rest against the caster frame when you release the wheel lock or SStteeeerr--LLoocckk (Figure 13). NNoottee -- You can apply a wheel lock or SStteeeerr--LLoocckk from the head end or foot end of the cot. FFiigguurree 1111 WWhheeeell lloocckk oonn FFiigguurree 1122 SStteeeerr--LLoocckk oonn FFiigguurree 1133 WWhheeeell lloocckk aanndd SStteeeerr--

LLoocckk ooffff RRoolllliinngg tthhee ccoott wwiitthh aa ppaattiieenntt WWAARRNNIINNGG Always transport the cot at transport height or the lowest possible height to reduce the risk of a cot tip. If possible, obtain additional assistance or take an alternate route. Always avoid high obstacles, such as curbs, steps, or rough terrain to avoid the risk of a cot tip or injury. Always center the patient and equipment or accessories. Lock adjustable features and intended lift points before you transport a patient on the product. Do not apply a wheel lock when a patient is on the product or when you move the product to avoid the risk of a cot tip or injury. Always use the specified push/pull locations to reduce the risk of a cot tip or injury. Always stow and latch the transport handle before you load, unload, or use the transport handle to lift the cot. CCAAUUTTIIOONN -- Do not use siderails as a patient restraint device. To roll the cot with a patient:

1. Press the release or transport height button. NNoottee For patients who weigh 500 lb (227 kg) or less, use the transport height feature. For patients who weigh more than 500 lb (227 kg), transport at the lowest possible height. 2. Position one operator at the foot end and one operator at the head end of the cot. 3. Apply SStteeeerr--LLoocckk (see ApplyingorreleasingawheellockorSteer-Lock (page 29)). 4. Check that the litter is perpendicular when you approach door sills or other low obstacles. 5. Lift each set of transport wheels over the door sill or obstacle separately. PPuusshhiinngg oorr ppuulllliinngg tthhee ccoott wwiitthh tthhee ttrraannssppoorrtt hhaannddllee WWAARRNNIINNGG Always transport the cot at transport height or the lowest possible height to reduce the risk of a cot tip. If possible, obtain additional assistance or take an alternate route. Always avoid high obstacles, such as curbs, steps, or rough terrain to avoid the risk of a cot tip or injury. EN 30 6507-009-001 Rev AB.3 ABC Always center the patient and equipment or accessories. Lock adjustable features and intended lift points before you transport a patient on the product. Do not apply a wheel lock when a patient is on the product or when you move the product to avoid the risk of a cot tip or injury. Always use the specified push/pull locations to reduce the risk of a cot tip or injury. Always stow and latch the transport handle before you load, unload, or use the transport handle to lift the cot. To push or pull the cot:

1. Press either one of the transport handle latch buttons and pull out the transport handle. 2. Check that the litter is perpendicular when you approach door sills or other low obstacles. 3. Lift each set of transport wheels over the door sill or obstacle separately. NNoottee -- You can also lock the transport handle in the 90 degree upright position to push or pull the cot. See Figure 14, Figure 15, and Figure 16 for transport handle locking positions. FFiigguurree 1144 SSttoowweedd ((rreettrraacctteedd)) FFiigguurree 1155 AAnngglleedd ((eexxtteennddeedd)) FFiigguurree 1166 VVeerrttiiccaall ((eexxtteennddeedd)) LLooaaddiinngg tthhee ccoott iinnttoo aa vveehhiiccllee Always load an occupied cot with a minimum of two trained operators. Two operators must be present when a cot is occupied. Operators must be able to lift the total weight of the patient, cot, and any items on the cot. WWAARRNNIINNGG Always support the load of the patient, cot, and accessories after the weight is off of the ground. Always use two operators when a cot is occupied. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Do not load the cot into a vehicle with the head section retracted when using a cot fastener. The cot may tip or not connect with the cot fastener. Always make sure that the cot is locked in the cot fastener before you load and unload. Injury may occur if the cot is not secure. Always try to load and unload the cot on level ground to reduce the risk of a cot tip or injury. Do not use the jog function to jog past the set cot load height after the cot safety bar connects with the vehicle safety hook. Always operate the cot only when all persons are clear of the mechanisms. Entanglement in powered cot mechanisms can cause serious injury. Always stow and latch the transport handle before you load, unload, or use the transport handle to lift the cot. CCAAUUTTIIOONN -- Always clear any obstacles that may interfere and cause injury to the operator or patient before operating the product. Stryker recommends that both operators are at the foot end to reduce the load on each operator. One or two operators can lift from the foot end of the cot. The operator must be able to lift the cot high enough for the cot legs to extend when the cot is unloaded. 6507-009-001 Rev AB.3 31 EN NNoottee You can load an unoccupied cot into a vehicle with one operator using the powered method. For information about using your cot with PPoowweerr--LLOOAADD, see the PPoowweerr--LLOOAADD Operations Manual. To load a cot into a vehicle with an antler style cot fastener:

1. Extend and lock the retractable head section. 2. Stow and latch the transport handle. 3. Place the cot in a loading position. NNoottee -- A loading position is any position where the load wheels meet the vehicle floor height. 4. Lift the vehicle bumper, if equipped, to the raised position. 5. Roll the cot to the open door of the vehicle patient compartment. 6. Push the cot forward until the load wheels are on the vehicle patient compartment floor and the cot safety bar passes the vehicle safety hook. 7. Pull the cot back until the cot safety bar connects to the vehicle safety hook for maximum clearance to lift the base. 8. Check that the cot safety bar connects with the vehicle safety hook. 9. Load the cot. NNoottee -- Always use the powered method to load an unoccupied cot with one operator. Do not use the manual method to load an unoccupied cot with one operator. Powered method - using the cot control switches:

With both operators at the foot end

(recommended method) With one operator at the foot end and one operator on the side With one operator (when loading an unoccupied cot) Grasp the cot frame at the foot end and press and hold the retract (-) button to retract the cot undercarriage. a. Both operators: Grasp the cot frame at the foot end. b. Operator 1: Press and hold the retract (-) button to retract the cot undercarriage. a. Operator 1: Grasp the cot frame at the foot end and press and hold the retract (-) button to retract the cot undercarriage. b. Operator 2: Grasp the cot outer rail to stabilize the cot as the cot undercarriage retracts. Manual method - using the manual back-up release handle:

a. Operator 1 (at the foot end):

i. Grasp the cot frame at the foot end. ii. Lift the foot end of the cot until you lift the weight off of the cot base. iii. Squeeze and hold the manual back-up release handle. b. Operator 2 (on the side):

i. Grasp the cot outer rail to stabilize the cot as you retract the cot undercarriage. ii. Raise the cot undercarriage to the highest height position. 10. Push the cot into the vehicle patient compartment. Check that the foot section does not protrude from the vehicle or hit the door. 11. Make sure that the cot is locked into the cot fastener (not included) by firmly pulling side to side on the foot end of the cot. NNoottee -- When you use the manual back-up release handle, do not lift the base rapidly or the movement may appear sluggish. Lift with a slow, constant motion. EN 32 6507-009-001 Rev AB.3 UUnnllooaaddiinngg tthhee ccoott ffrroomm aa vveehhiiccllee Always unload an occupied cot with a minimum of two trained operators. Operators must be able to lift the total weight of the patient, cot, and any items on the cot. WWAARRNNIINNGG Always support the load of the patient, cot, and accessories after the weight is off of the ground. Always use two operators when a cot is occupied. Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. Always make sure that the cot safety bar connects with the vehicle safety hook before you remove the cot from the vehicle patient compartment to avoid the risk of injury. Do not pull or lift on the cot safety bar when you unload the cot. Always make sure that the cot is locked in the cot fastener before you load and unload. Injury may occur if the cot is not secure. Always try to load and unload the cot on level ground to reduce the risk of a cot tip or injury. Do not use the jog function to jog past the set cot load height after the cot safety bar connects with the vehicle safety hook. Always operate the cot only when all persons are clear of the mechanisms. Entanglement in powered cot mechanisms can cause serious injury. Always stow and latch the transport handle before you load, unload, or use the transport handle to lift the cot. CCAAUUTTIIOONN Always set the transport wheels safely on the ground when you unload the cot from the vehicle patient compartment to avoid the risk of product damage. Always clear any obstacles that may interfere and cause injury to the operator or patient before operating the product. One or two operators can lift from the foot end of the cot. The operator must be able to lift the cot high enough for the cot legs to extend when the cot is unloaded. NNoottee -- You can unload an unoccupied cot from a vehicle with one operator. To unload the cot from a vehicle:

1. Lift the vehicle bumper, if equipped, to the raised position. NNoottee -- The cot is equipped with bumper detection. An obstruction will stop the cot from moving even if you continue to hold the extend button. Remove the obstruction and press the extend button again to continue unloading. You may need to load the cot back into the vehicle to proceed. 2. Remove the cot from the cot fastener. 3. Unload the cot. Powered method - using the cot control switches:

6507-009-001 Rev AB.3 33 EN With both operators at the foot end With one operator at the foot end and one operator on the side With one operator (when unloading an unoccupied cot) a. Both operators: Grasp the cot frame at the foot end. b. Both operators: Pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. WWAARRNNIINNGG -- DDoo nnoott pprreessss tthhee eexxtteenndd ((++)) bbuuttttoonn uunnttiill tthhee ssaaffeettyy bbaarr ccoonnnneeccttss wwiitthh tthhee vveehhiiccllee ssaaffeettyy hhooookk.. c. Operator 2: Make sure that the safety bar connects with the vehicle safety hook. d. Operator 1: Depress the extend

(+) button to extend the cot undercarriage. e. Operator 2: Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. a. Operator 1: Grasp the cot frame at the foot end and pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. WWAARRNNIINNGG -- DDoo nnoott pprreessss tthhee eexxtteenndd ((++)) bbuuttttoonn uunnttiill tthhee ssaaffeettyy bbaarr ccoonnnneeccttss wwiitthh tthhee vveehhiiccllee ssaaffeettyy hhooookk.. b. Operator 2: Grasp the cot outer rail to stabilize the cot. c. Operator 1: Depress the extend

(+) button to extend the cot undercarriage. d. Operator 2: Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. Manual method - using the manual back-up release handle:

a. Grasp the cot frame at the foot end. b. Pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. WWAARRNNIINNGG -- DDoo nnoott pprreessss tthhee eexxtteenndd ((++)) bbuuttttoonn uunnttiill tthhee ssaaffeettyy bbaarr ccoonnnneeccttss wwiitthh tthhee vveehhiiccllee ssaaffeettyy hhooookk.. c. Depress the extend (+) button to extend the cot undercarriage. d. Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. With both operators at the foot end

(recommended method) With one operator at the foot end and one operator on the side With one operator (when unloading an unoccupied cot) a. Both operators: Grasp the cot frame at the foot end. b. Operator 1: Pull the manual back-up release handle to extend the cot undercarriage. Pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. Release the manual back-up release handle when the base is fully extended. c. Operator 2: Make sure that the safety bar connects with the vehicle safety hook. Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. a. Operator 1: Grasp the cot frame at the foot end. Pull the manual back-up release handle to extend the cot undercarriage. Pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. Release the manual back-up release handle when the base is fully extended. b. Operator 2: Make sure that the safety bar connects with the vehicle safety hook. Grasp the cot outer rail to stabilize the cot. Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. a. Grasp the cot frame at the foot end. b. Pull the manual back-up release handle to extend the cot undercarriage. c. Pull the cot out of the vehicle patient compartment until the safety bar connects with the vehicle safety hook. d. Release the manual back-up release handle when the base is fully extended. e. Pull the safety bar release lever forward to remove the safety bar from the vehicle safety hook. PPoossiittiioonniinngg ooppeerraattoorrss aanndd hheellppeerrss WWAARRNNIINNGG -- Always follow proper hand placement on hand grips. Keep all hands clear of the red safety bar pivots when you load, unload, or change the cot height position. EN 34 6507-009-001 Rev AB.3 CChhaannggiinngg lleevveellss RRoolllliinngg LLooaaddiinngg aanndd uunnllooaaddiinngg Two operators (O) Two helpers (H) Two operators (O) Four helpers (H) RRaaiissiinngg oorr lloowweerriinngg tthhee bbaacckkrreesstt To raise the backrest, squeeze the backrest adjustment handle to move the backrest to the desired height. To lower the backrest, squeeze the backrest adjustment handle while you push down on the backrest to the desired height. RRaaiissiinngg oorr lloowweerriinngg tthhee ssiiddeerraaiillss Always lower the siderails when you transfer a patient to the cot or from the cot. CCAAUUTTIIOONN Do not use siderails as a patient restraint device. Do not use siderails as a push/pull device or to steer the product. To raise the siderails, lift up on the siderail until the latch clicks and the siderail locks into place. Always keep the siderails in the raised position unless you are transferring the patient. To lower the siderails, squeeze the siderail release handle to release the siderail latch. Guide the siderail down toward the foot end of the cot until the siderail lays flat. Always lower the siderails when you transfer a patient to or from the cot. RRaaiissiinngg oorr lloowweerriinngg tthhee ssiiddeerraaiillss ((XXPPSS ooppttiioonn)) You can order your cot with the expandable patient surface (XPS) option or upgrade your cot to add the XPS option. CCAAUUTTIIOONN Do not use siderails as a patient restraint device. Do not sit or stand on the siderails (XPS option). Do not use the siderails (XPS option) as a patient transfer device or surface (for example, to slide a patient from the cot to another surface). Do not position patients with full weight on the siderails (XPS option). 6507-009-001 Rev AB.3 35 EN HHOOHHOOOOHHHHHHOOOOHHHHHHHHOO Do not use the siderails as a push/pull device or to steer the product. Siderails (XPS option) attach to the cot and are always available for your use. The siderails (XPS option) adjust according to patient size and lock into seven positions. The siderails also adjust to fit through standard doorways or elevators. To raise the siderails, lift up on the siderail until locked into the desired position. To lower the siderails, lift up to relieve the weight, then pull the red lever. Always lower the siderails when you transfer a patient to or from the cot. The XPS option is not a primary patient support surface. It includes a wider mattress and is intended to enhance patient comfort. EExxtteennddiinngg oorr rreettrraaccttiinngg tthhee rreettrraaccttaabbllee hheeaadd sseeccttiioonn Extend the retractable head section before you load the cot into the vehicle patient compartment. Retract the retractable head section to roll the cot in any direction on the load wheels for improved mobility and maneuverability, even in the lowest position. WWAARRNNIINNGG Always lock the head and foot sections into place before you operate the cot. Do not load the cot into a vehicle with the head section retracted when using a cot fastener. The cot may tip or not connect with the cot fastener. To extend or retract the retractable head section:

1. Grasp the outer rail with one hand for support and pull the head section release handle. Rotate the head section release handle toward the head end of the cot to release the head section from the locked position. 2. While you hold the head section release handle in the released position, pull the head section away from the litter frame. Extend or push the head section toward the litter frame to retract. 3. Release the head section release handle to lock the head section in either the extended or retracted position. 4. Pull the head section up and down to check that it is locked. EExxtteennddiinngg oorr rreettrraaccttiinngg tthhee rreettrraaccttaabbllee ffoooott sseeccttiioonn WWAARRNNIINNGG -- Always lock the head and foot sections into place before you operate the cot. To extend or retract the retractable foot section:

1. Grasp the outer rail with one hand for support and pull the foot section release lever. 2. While you hold the foot section release lever, pull the foot section away from the litter frame. Extend or push the foot section toward the litter frame to retract. 3. Release the foot section release lever to lock the foot section in either the extended (Figure 17), mid (Figure 18), or retracted position (Figure 19). 4. Pull the foot section up and down to check that it is locked. EN 36 6507-009-001 Rev AB.3 FFiigguurree 1177 EExxtteennddeedd FFiigguurree 1188 MMiidd FFiigguurree 1199 RReettrraacctteedd RRaaiissiinngg oorr lloowweerriinngg tthhee ffoooottrreesstt You can adjust the footrest to elevate the patients legs. To raise the footrest, lift the frame as high as possible. The support bracket automatically secures the frame when you release the footrest. To lower the footrest, lift the frame and lift up on the footrest release handle (B) until the frame releases the support bracket

(Figure 20). Lower the footrest until flat. RRaaiissiinngg oorr lloowweerriinngg tthhee kknneeee GGaattcchh To raise the knee Gatch:

1. Lift either of the red lifting loops (A) until the knee Gatch is in the highest position (Figure 20). 2. Lower the knee Gatch to secure the support bracket to the locking mechanism. 3. Check that the locking mechanism is secure before you release the red lifting loop. To lower the knee Gatch, lift either of the red lifting loops (A) to relieve pressure on the locking mechanism. While you hold the red lifting loop, push on the red footrest release handle (B) until the support bracket is released. Lower the knee Gatch until flat. To raise the knee Gatch in trend, lift the footrest frame (C) as high as possible until the frame locks into place. The support bracket automatically connects when you release the frame. To lower the knee Gatch in trend, lift the footrest frame (C). While you hold the frame, lift up on the red footrest release handle (B) until the frame releases the support bracket. Lower the footrest until flat. 6507-009-001 Rev AB.3 37 EN SSeeccuurriinngg tthhee ppaattiieenntt wwiitthh tthhee rreessttrraaiinntt ssttrraappss FFiigguurree 2200 GGaattcchh Secure restraint straps to the cot in the required attachment locations: shoulders, waist, thighs, and ankles. PPoowweerr--PPRROO 2 cots are compatible with the X-restraint strap system. WWAARRNNIINNGG Always use all restraint straps to secure the patient on the product. An unrestrained patient may fall from the product and be injured. Do not attach restraint straps to the base tubes, cross tubes, or litter skin. CCAAUUTTIIOONN -- Do not entangle the restraint straps in the base frame when you raise or lower the cot. NNoottee -- Restraint straps are a Type BF applied part. Restraint strap attachment locations should provide strong anchorage and proper restraint position (Figure 21). If you do not use the restraint strap attachment locations shown below, the cot is not crash-rated. Do not allow restraint straps to interfere with equipment or accessories. Buckle the restraints across the shoulders, waist, thighs, and ankles. Buckle all restraint straps when the cot is not in use. 1. Attachingtheshoulderrestraints (page 39) 2. Attachingthewaistrestraints (page 40) 3. Attachingthethighrestraints (page 40) 4. Attachingtheanklerestraints (page 41) EN 38 6507-009-001 Rev AB.3 ABC FFiigguurree 2211 RReessttrraaiinntt ssttrraapp aattttaacchhmmeenntt llooccaattiioonnss AAttttaacchhiinngg tthhee sshhoouullddeerr rreessttrraaiinnttss To attach the X-restraint shoulder restraints (Figure 22):

1. Wrap the restraint around the cot frame where the matching label is located (Figure 23). 2. Pull the restraint buckle through the loop, toward the head end of the cot. 3. Feed the buckle under the XPS system. 4. Pull the restraint through tight and toward the back of the backrest. 5. Feed the buckle through the opening in the backrest. 6. Connect the patient right shoulder buckle to the patient left waist buckle. 6507-009-001 Rev AB.3 39 EN 1243 FFiigguurree 2222 AAttttaacchhiinngg tthhee sshhoouulldd rreessttrraaiinnttss FFiigguurree 2233 SShhoouullddeerr rreessttrraaiinnttss llooccaattiioonn AAttttaacchhiinngg tthhee wwaaiisstt rreessttrraaiinnttss To attach the X-restraint waist restraints:

1. Wrap the restraint around the cot frame where the matching label is located (Figure 24). 2. Pull the restraint buckle through the loop, toward the head end of the cot. 3. Feed the buckle under the XPS system. 4. Pull the buckles tight. One restraint should angle toward the head end and one should lay straight across the cot. 5. Connect the patient right buckle to the patient left buckle. FFiigguurree 2244 WWaaiisstt rreessttrraaiinntt llooccaattiioonn AAttttaacchhiinngg tthhee tthhiigghh rreessttrraaiinnttss To attach the X-restraint thigh restraint:

1. Wrap the restraint around the cot frame where the matching label is located (Figure 25). 2. Pull the restraint buckle through the loop, toward the head end of the cot. 3. Pull the restraint tight. 4. Connect the patient right buckle to the patient left buckle. EN 40 6507-009-001 Rev AB.3 123456 FFiigguurree 2255 TThhiigghh rreessttrraaiinntt llooccaattiioonn AAttttaacchhiinngg tthhee aannkkllee rreessttrraaiinnttss To attach the X-restraint ankle restraints:

1. Wrap the restraint around the cot frame where the matching label is located (Figure 26). 2. Pull the restraint buckle through the loop, toward the head end of the cot. 3. Pull the buckle tight. 4. Connect the patient right buckle to the patient left buckle. AAddjjuussttiinngg rreessttrraaiinntt ssttrraappss FFiigguurree 2266 AAnnkkllee rreessttrraaiinntt llooccaattiioonn Open the restraint straps and place them at either side of the cot while you position the patient on the cot mattress. Lengthen the restraint straps, buckle them around the patient, and shorten them to tighten. To open the restraint strap, press the red button on the front of the buckle receiver. This allows you to release the buckle latch plate and pull it out of the receiver. To close the restraint strap, push the latch plate into the receiver until you hear a click. To lengthen the restraint strap, grasp the buckle latch plate, turn it at an angle to the webbing, then pull it out. A hemmed tab at the end of the webbing prevents the latch plate from coming off of the strap. To shorten the restraint strap, grasp the hemmed tab and pull the webbing back through the latch plate to tighten. When you buckle a restraint strap around a patient, secure the latch plate and remove any loose webbing from the cot. Inspect the restraint straps at least once a month (more if used often). Check for a bent or broken receiver or latch plate, or torn or frayed webbing. Replace any worn or inoperable restraint strap. 6507-009-001 Rev AB.3 41 EN AAddddiinngg aa rreessttrraaiinntt ssttrraapp eexxtteennssiioonn Add a restraint strap extension (6082-160-050) for extra length when you buckle the lap belt around larger patients. FFiigguurree 2277 RReessttrraaiinntt ssttrraapp eexxtteennssiioonn SSeeccuurriinngg tthhee cchhiilldd rreessttrraaiinntt wwiitthh tthhee XX--rreessttrraaiinntt ppaacckkaaggee To attach the Britax Meridian SICT (series no. 7200/A/2010), Platinum Pro SICT (series no. 7200/A/2013i), and Millenia SICT (series no. 7200/A/2013/i) Convertible Child Restraint to the cot with the X-restraint package (6500-001-430):

1. Lay the cot flat. 2. Open the waist restraint straps (6500-001-402 and 6500-001-403). Lay the straps to the side and out of the way. 3. Position the child restraint to face the foot end of the cot. 4. Place the child restraint in the reclined position. 5. Raise the cot Fowler up to align with the back of the child restraint. 6. Loop the upper anchorage strap with the anchor fitting and attachment clip from the child restraint around the cot Fowler

(Figure 28). Pull the adjustment strap to tighten and remove slack. 7. Pull the waist restraint under the siderail and through the bottom of the child restraint (Figure 29). FFiigguurree 2288 AAnncchhoorraaggee ssttrraapp llooccaattiioonn FFiigguurree 2299 SSeeccuurree tthhee wwaaiisstt rreessttrraaiinntt 8. While firmly pushing down on the seat, pull the waist restraint with your other hand to tighten. 9. Attach one restraint strap (6500-001-404) to the foot end extension tube (Figure 30). NNoottee -- The foot end extension tube must be in the mid or extended position (see Extendingorretractingtheretractable footsection (page 36)). EN 42 6507-009-001 Rev AB.3 FFiigguurree 3300 AAttttaacchh ttoo tthhee ffoooott eenndd eexxtteennssiioonn ttuubbee 10. Pull the restraint strap (6500-001-404) through the foot end of the child restraint (Figure 31). 11. While firmly pushing down on the seat, pull the restraint with your other hand to tighten. 12. While holding the tension, close the rear facing lock-off on the buckle side (Figure 32). FFiigguurree 3311 RReessttrraaiinntt llooccaattiioonn FFiigguurree 3322 RReeaarr ffaacciinngg lloocckk--ooffff 13. Close the rear facing lock-off on the opposite side. 14. Place the baby into the child restraint and secure per the manufacturers instructions. HHaannggiinngg eeqquuiippmmeenntt ffrroomm tthhee eeqquuiippmmeenntt hhooookk Use the equipment hook to hang additional accessories or equipment, such as defibrillators and monitors. CCAAUUTTIIOONN Do not load the equipment hook above the safe working load of 35 lb (15.8 kg). Always remove all accessories or equipment from the equipment hook when in the vehicle. 6507-009-001 Rev AB.3 43 EN PPoossiittiioonniinngg tthhee ttwwoo--ssttaaggee IIVV ppoollee ooppttiioonn FFiigguurree 3333 EEqquuiippmmeenntt hhooookk CCAAUUTTIIOONN -- Do not load the IV pole above the safe working load of 25 lb (11.3 kg). To position the IV pole (Figure 34):

1. Lift and pivot the IV pole from the storage position. Push down until the IV pole locks into the receptacle (A). 2. To raise the height of the IV pole, turn the locking collar (B) counterclockwise and pull up on the telescoping section (C). Raise the IV pole to the desired height. 3. Turn the locking collar (B) clockwise to lock the telescoping section in place. 4. Hang the IV bags on the IV hook (D). 5. Turn the locking collar (B) counterclockwise and slide the telescoping section (C) into the bottom tube. 6. Turn the locking collar (B) clockwise to tighten. 7. Lift up and pivot the pole down into the storage position. EN 44 6507-009-001 Rev AB.3 PPoossiittiioonniinngg tthhee tthhrreeee--ssttaaggee IIVV ppoollee ooppttiioonn FFiigguurree 3344 TTwwoo--ssttaaggee IIVV ppoollee CCAAUUTTIIOONN -- Do not load the IV pole above the safe working load of 25 lb (11.3 kg). To position the IV pole (Figure 35):

1. Lift and pivot the IV pole from the storage position. Push down until the IV pole locks into the receptacle (A). 2. To raise the height of the IV pole, turn the locking collar (B) counterclockwise and pull up on the telescoping section (C). Raise the IV pole to the desired height. 3. Turn the locking collar (B) clockwise to lock the telescoping section in place. 4. For a higher IV pole, pull up on section (D) until the spring clip (E) connects. 5. Hang the IV bags on the IV hook (F). 6. To lower the IV pole, push in on the spring clip (E) and slide section (D) down into section (C). Turn the locking collar (B) counterclockwise and slide section (C) into the bottom tube. 7. Turn the locking collar (B) clockwise to tighten. 8. Lift up and pivot the pole down into the storage position. 6507-009-001 Rev AB.3 45 EN CDAB AAttttaacchhiinngg aann ooxxyyggeenn bboottttllee ttoo tthhee ooxxyyggeenn bboottttllee hhoollddeerr ooppttiioonn FFiigguurree 3355 IIVV ppoollee rraaiisseedd ppoossiittiioonn CCAAUUTTIIOONN Do not load the oxygen bottle holder above the safe working load of 15 lb (6.8 kg). Do not use two oxygen bottle holders at the same time. To attach an oxygen bottle to the oxygen bottle holder:

1. Place an oxygen bottle in the holder. 2. Insert the lower strap through the buckle and affix the strap onto itself to secure the oxygen bottle to the holder. NNoottee Do not use the oxygen bottle holder to hold an oxygen bottle holder when the transport vehicle is in motion. Always place the oxygen bottle holder in an appropriate storage location when the transport vehicle is in motion. Inspect the straps and clips for wear between use. Replace the strap if it no longer holds the oxygen bottle. AAttttaacchhiinngg tthhee bbaassee ssttoorraaggee nneett ooppttiioonn CCAAUUTTIIOONN Do not load the base storage net above the safe working load of 20 lb (9 kg). Always be careful when you retract the base to avoid damaging items that are stored in the base storage net. To attach the base storage net, wrap the VVeellccrroo straps around the base tubes. EN 46 6507-009-001 Rev AB.3 ABCDEFABEDCF AAttttaacchhiinngg tthhee bbaacckkrreesstt ssttoorraaggee ppoouucchh ooppttiioonn CCAAUUTTIIOONN Do not load the single-sided backrest storage pouch above the safe working load of 10 lb (4.5 kg). Do not load the dual-sided backrest storage pouch above the safe working load of 20 lb (9 kg). Do not allow the storage pouch to interfere with the operation of the retractable head section. To attach the single-sided or dual-sided backrest storage pouch:

1. Insert each strap through a opening in the backrest skin. 2. Mount the pouch flat against the backrest. 3. Secure the backrest storage pouch to the cot with the VVeellccrroo straps. NNoottee -- Only secure the VVeellccrroo straps that correspond to the selected attachment side of the cot. Secure the VVeellccrroo straps that are not in use to themselves. AAttttaacchhiinngg tthhee hheeaadd eenndd ssttoorraaggee ffllaatt ooppttiioonn WWAARRNNIINNGG -- Do not allow the head end storage flat to interfere with the operation of the retractable head section, safety bar, or vehicle safety hook. CCAAUUTTIIOONN -- Do not load the head end storage flat above the safe working load of 40 lb (18 kg). To attach the head end storage flat (Figure 36):

1. Attach the VVeellccrroo straps (A) near the pneumatic cylinder and around the cross tube (C) of the retractable head section. 2. Buckle the restraint straps (B) around the outer rails of the retractable head section. AAttttaacchhiinngg tthhee mmaattttrreessss FFiigguurree 3366 HHeeaadd eenndd ssttoorraaggee ffllaatt WWAARRNNIINNGG Always secure the mattress to the product to avoid movement during patient transfer. Do not store items under the mattress. Items under the mattress may interfere with product operation. The following mattress options are compatible with this product:

Standard Gatch bolster mattress (6506-002-150) - use with the standard siderail 6507-009-001 Rev AB.3 47 EN ABAB Gatch bolster mattress (6506-003-130) - use with the expandable patient surface (XPS) option To attach the mattress to the cot:

1. Align the VVeellccrroo on the back of the mattress with the VVeellccrroo on the cot litter. 2. Attach the strap at the foot end of the mattress through the two holes in the foot end skin on the cot litter. 3. Pull the strap through the buckle and attach the VVeellccrroo to secure the strap. NNoottee -- The mattress is a Type BF applied part. IInnsseerrttiinngg tthhee bbaatttteerryy To maximize available battery power, only use batteries that have been charged within the last 48 hours. To insert the battery:

1. Align the tabs in the battery enclosure. 2. Push the battery into the enclosure until the latch clicks into place. RReemmoovviinngg tthhee bbaatttteerryy ffrroomm tthhee pprroodduucctt After you discharge the battery, remove it from the product and replace it with a charged battery. WWAARRNNIINNGG Do not remove the battery when the product is active. Do not attempt to open the battery pack for any reason, to avoid the risk of electric shock. If the battery pack case is cracked or damaged, do not insert it into the charger. Return damaged battery packs to a service center for recycling. Always avoid direct contact with a wet battery or battery enclosures. Contact may cause injury to the patient or operator. CCAAUUTTIIOONN -- Always remove the battery if you do not intend to use the product for more than 24 hours or longer. Running the battery repeatedly, without rest periods, can increase the temperature within the cells and reduce life. For example, lifting a heavy patient up and down several times in rapid succession can reduce the battery life. To remove the battery from the product:

1. Press the battery release button (A) to release the battery from the product (Figure 37). 2. Slide the released battery out of the enclosure. EN 48 6507-009-001 Rev AB.3 SSttoorriinngg tthhee bbaatttteerryy FFiigguurree 3377 BBaatttteerryy rreelleeaassee bbuuttttoonn For the longevity, performance, and safety of this equipment, use the original packaging materials when you store or transport this equipment. All batteries lose charge during storage or periods of inactivity. The battery can lose up to 30 percent of its charge within 48 hours after you remove it from the charger. Use and fully charge stored batteries every three months to maintain top performance. CChhaarrggiinngg tthhee bbaatttteerryy WWAARRNNIINNGG Do not insert a cracked or damaged battery into the charger. Return damaged batteries to a service center for recycling. Do not connect AC and DC power supplies to the battery at the same time to avoid the risk of fire or electric shock. NNoottee -- For extended storage, store the battery on the charger to trickle charge. The charger keeps the battery charged and ready for use. To charge the battery:

1. Insert a clean, dry battery into the charger. Check that the battery is locked into the charger. NNoottee When the battery is charged and ready for use, the battery power indicator will show four LEDs. The maximum charge time is 4 hours. 2. Press the battery release button (A) and slide the charged battery out of the charger (Figure 38). 6507-009-001 Rev AB.3 49 EN A EElleeccttrriiccaall ppoowweerr rreeqquuiirreemmeennttss FFiigguurree 3388 CChhaarrggiinngg tthhee bbaatttteerryy For reliable and effective operation, reference the following electrical power requirements when you configure the electrical power source for the charger. PPoowweerr ttyyppee OOppeerraattiioonnaall vvoollttaaggee rraannggee FFrreeqquueennccyy MMaaxxiimmuumm ccuurrrreenntt ddrraaww SSttaannddbbyy ccuurrrreenntt ddrraaww LLooww vvoollttaaggee sshhuutt ooffff AC DC 100-240 VAC, 50/

60 Hz, 1A 50/60 Hz

< 1.2A

< 50 mA 90 VAC 12-34 VDC, 5A Not applicable

< 6.67A

< 150 mA 10 VDC CChhaarrggeerr sseettuupp During setup, place the charger in an environmentally controlled location that is:

Free of dust and moisture Kept within a constant temperature range (see Specifications-Alvarium (page 13)) Readily accessible for use Locate and maintain the power supply and power cords to minimize the risk of damage and inadvertent disconnections. SSeeccuurriinngg tthhee mmoouunnttiinngg ppllaattee ooppttiioonn WWAARRNNIINNGG Always have a certified mechanic, familiar with ambulance vehicle construction, secure the mounting plate option and charger. Always make sure that the mounting plate option is secured to the surface before use. To secure the mounting plate to a surface (Figure 39):

1. Use the mounting plate as a template to mark the location of the mounting holes (A). 2. Position the mounting plate and check that the:

a. Spring tab (B) is located at the rear of the charger. NNoottee -- When mounting to a vertical surface, the spring tab should be horizontal and pointed to the left. EN 50 6507-009-001 Rev AB.3 A FFiigguurree 3399 MMoouunnttiinngg PPllaattee b. Power cord easily plugs into the rear of the charger. c. Charger slides from front to back to connect to the plate after mounting. d. Mounting plate is secured correctly for the ambulance or station location:

AAmmbbuullaannccee llooccaattiioonn ((AACC oorr DDCC ppoowweerr)) SSttaattiioonn llooccaattiioonn ((AACC ppoowweerr)) Secure the plate to a horizontal surface or shelf with size #10, grade 5 flat head screws minimum (not supplied). Secure the plate to a horizontal or vertical surface with size #10, grade 5 flat head screws minimum (not supplied). Check that the selected mounting surface is strong enough to support the charger and battery during transport. Allow for easy battery insertion and removal. Locate the power supply within reach of the power cord. For vertical securement, position the mounting plate with the spring tab directly below the mounting screws, so the battery remains supported by the charger even if the battery release button is accidentally pressed. Allow for easy battery insertion and removal. SSeeccuurriinngg tthhee cchhaarrggeerr ttoo tthhee mmoouunnttiinngg ppllaattee ooppttiioonn To secure the charger to the mounting plate (Figure 40):

1. Move the red AC/DC slider (A) to the center position. Avoid interference between the hook features and charger mount spring. 2. Align the rear keyway slots (B) onto the mounting plate fasteners (C). 3. Slide the charger (D) onto the mounting plate (E) until locked. 6507-009-001 Rev AB.3 51 EN AB FFiigguurree 4400 SSeeccuurriinngg tthhee cchhaarrggeerr ttoo tthhee mmoouunnttiinngg ppllaattee PPoowweerriinngg tthhee cchhaarrggeerr CCAAUUTTIIOONN Always place the electrical charger power cord where it will not be stepped on, tripped over, or otherwise subjected to damage or stress. Do not touch the battery receptacle terminals with metal objects. To power the charger (Figure 41):

1. Locate the power connection on the back of the charger. 2. Move the red AC/DC slider to expose the port and select the desired voltage configuration (AC or DC). A B C FFiigguurree 4411 CChhaarrggeerr rreeaarr vviieeww AC input Red AC/DC slider DC input 3. 4. Insert the power cord into the exposed charger port. Insert the other end of the charger power cord into a clean, uninterruptible power source. NNoottee -- Use only Stryker approved parts to power the charger. EN 52 6507-009-001 Rev AB.3 CDABECAB DDiissccoonnnneeccttiinngg tthhee cchhaarrggeerr CCAAUUTTIIOONN -- Always grasp and pull the plug, not the cord, when you disconnect the charger to avoid the risk of damage to the electrical plug and cord. To disconnect the charger, unplug the power cord from the AC or DC power source. 6507-009-001 Rev AB.3 53 EN AAcccceessssoorriieess aanndd ppaarrttss These accessories may be available for use with your product. Confirm availability for your configuration or region. Call Stryker Customer Service: 1-800-327-0770. NNaammee Belt extension Charger mounting plate HHAAVVAASSUU IV pole, two-stage, left HHAAVVAASSUU IV pole, two-stage, right HHAAVVAASSUU IV pole, three-stage, left HHAAVVAASSUU IV pole, three-stage, right Kit, MTS sensor assembly Mattress, knee Gatch bolster Mattress, knee Gatch bolster, grey Mattress, knee Gatch bolster, XPS Mattress, knee Gatch bolster, XPS, grey Oxygen bottle holder, Fowler Oxygen bottle holder, head section Restraint package, X-restraint Restraint package, X-restraint, blue Siderail, standard Siderail, XPS option Storage flat, head end Storage net, base Storage pouch, backrest, dual-sided Storage pouch, backrest, single-sided Wheel lock option, two Wheel lock option, four NNuummbbeerr 6082-160-050 650700450031 650700350005 650700350001 650700350006 650700350002 650707000001 6500-002-150 6506-002-150 6500-003-130 6506-003-130 650700450053 650700450054 6500-001-430 6500-001-431 650709990002 650709990001 6500-128-000 6500-160-000 650700450134 650700450142 650709990009 650709990010 Use only Stryker-approved parts. Other parts may result in increased electromagnetic emissions or decreased electromagnetic immunity of the system. Do not modify parts. Failure to comply may result in injury. NNaammee PPoowweerr ccoommppoonneennttss -- AACC Battery Battery (2x) Charger EN 54 NNuummbbeerr 650700080301 650700080302 650700450301 6507-009-001 Rev AB.3 NNaammee Power cord, Argentina Power cord, Australia Power cord, Brazil Power cord, China Power cord, Europe Power cord, Israel Power cord, Japan Power cord, North America Power cord, South Africa Power cord, Switzerland Power cord, United Kingdom PPoowweerr ccoommppoonneennttss -- DDCC 12 VDC cable, automotive NNuummbbeerr 650700450212 650700450105 650700450109 650700450108 650700450103 650700450210 650700450106 650700450102 650700450211 650700450107 650700450104 650700450101 6507-009-001 Rev AB.3 55 EN CClleeaanniinngg aanndd ddiissiinnffeeccttiinngg wwiitthh wwiippeess For United States only. Confirm availability for your configuration or region. Call Stryker Customer Service: 1-800-327-

0770. Strykers preferred wipes (2060-000-001 6'' x 10'' or 2060-000-002 9'' x 12'') include the following active ingredients:

n-Alkyl (60% C14, 30% C16, 5% C12, 5% C18) dimethyl benzyl ammonium chloride - 0.154%

n-Alkyl (68% C12, 32% C14) dimethyl ethylbenzyl ammonium chloride - 0.154%

Isopropanol - 21.000%

Non-active ingredient: Ethylene Glycol Monobutyl Ether < 3%

NNoottee -- For safety information, read the product label. To clean or disinfect the external product surface:

1. To clean, wipe external surfaces with a fresh, clean wipe to remove all visible soils. Repeat as necessary until the product is clean. NNoottee Use as many wipes as necessary. Complete step 1 before you disinfect. 2. To disinfect, wipe external surfaces with a fresh, clean wipe until wet. Allow the external surface to remain wet for two minutes at room temperature. 3. Allow the product to dry before you return it to service. EN 56 6507-009-001 Rev AB.3 CClleeaanniinngg tthhee pprroodduucctt WWAARRNNIINNGG Always follow these cleaning and disinfecting guidelines, in addition to your protocols, to maintain hygienic safety. Always use any appropriate personal protective equipment while power washing to avoid inhaling contagion. Power washing equipment may aerate contamination. CCAAUUTTIIOONN Always remove the battery before you wash the product. Do not clean, service, or perform maintenance while the product is in use. Do not steam clean or ultrasonically clean the product. Do not exceed 180 F (82 C) as the maximum water temperature. Do not exceed 1500 psi (130.5 bar) as the maximum water pressure. If you are using a hand held wand to wash the product, keep the pressure nozzle at a minimum of 24 in. (61 cm) from the product. The product is power washable. The product may show some signs of oxidation or discoloration from continuous washing. No degradation of the products performance will occur from power washing as long as you follow the proper procedures. Immersing restraint strap metal buckles can cause buckle corrosion and is not recommended. Rinse with clean water and allow to air dry to reduce chance of corrosion. Replace restraints if metal buckles are corroded. Direct skin contact with visibly soiled, permeable material may increase the risk of infection. Recommended cleaning method:

1. Remove the mattress and battery from the product. 2. Follow the disinfectant solution manufacturers dilution recommendations exactly. 3. Stryker recommends the standard hospital cart washer for power washing. 4. Allow the product to air dry. 5. Check functionality before you return the product to service. 6507-009-001 Rev AB.3 57 EN DDiissiinnffeeccttiinngg tthhee pprroodduucctt In general, when used in concentrations recommended by the manufacturer, either phenolic type or quaternary (excluding VViirreexx TB) type disinfectants can be used. Iodophor type disinfectants are not recommended for use because staining may occur. Recommended disinfectants:

Quaternary cleaners (active ingredient - ammonium chloride) that contain less than 3% glycol ether Phenolic cleaners (active ingredient - o-phenylphenol) Chlorinated bleach solution (5.25% - less than 1 part bleach to 100 parts water) 21% isopropanol alcohol Recommended disinfection method:

1. Follow the disinfectant solution manufacturers dilution recommendations exactly. 2. Hand wash all surfaces of the product with a disinfectant solution. 3. Avoid oversaturation and make sure that the product does not stay wet longer than the chemical manufacturers guidelines for proper disinfecting. 4. Allow the product to air dry. 5. Disinfect the VVeellccrroo after every use. Saturate the VVeellccrroo with disinfectant, rinse with water, and allow the disinfectant to evaporate. Appropriate disinfectant for nylon VVeellccrroo should be determined by the service. 6. Check functionality before you return the product to service. NNoottee Failure to follow the above directions when using these types of disinfectants may void this products warranty. Always wipe the product with clean water and dry after cleaning. Some cleaning products are corrosive in nature and may cause damage to the product. Failure to properly rinse and dry the product leaves a corrosive residue on the surface of the product and may cause premature corrosion of critical components. EN 58 6507-009-001 Rev AB.3 CClleeaanniinngg tthhee cchhaarrggeerr WWAARRNNIINNGG Always wear rubber gloves, in addition to personal protective equipment, when cleaning the battery to reduce the risk of injury. Always disconnect the charger from the wall outlet before cleaning to avoid the risk of electrical hazards. Do not spray fluid directly onto the charger. Do not power wash the charger. Do not use solvents, lubricants, or other chemicals to clean the charger unless otherwise directed. Do not immerse the charger in liquid or allow liquid to collect on top of the charger to avoid the risk of electric shock. To clean the charger:

1. Disconnect the charger from the wall outlet to avoid electrical hazards during cleaning. 2. Wipe surfaces of the charger with a soft cloth dampened with a non-abrasive, disinfectant solution (see Disinfectingthe product). 3. Wipe with a cloth moistened with clean water to remove any cleaning chemicals or residue. 4. Dry thoroughly before you return the charger to service. CClleeaanniinngg tthhee bbaatttteerryy WWAARRNNIINNGG Always wear rubber gloves, in addition to personal protective equipment, when cleaning the battery to reduce the risk of injury. Always use only non-conductive materials to wipe the battery. Always avoid excessive water exposure to the battery terminals. Do not directly handle or make contact with the battery terminals while cleaning to avoid the risk of injury. Do not immerse the battery in liquid or allow liquid to collect on top of the battery to avoid the risk of electric shock. Do not use solvents, lubricants, or other chemicals to clean the battery unless otherwise directed. Do not power wash the battery. CCAAUUTTIIOONN -- Do not steam clean or ultrasonically clean the product. To clean the battery:

1. Remove the battery from the product or charger. 2. Inspect the battery housing and terminal area for any cracks or damage. 3. Clean the battery with a disinfectant solution (see Disinfectingtheproduct). 4. Rinse the battery thoroughly with clean water to remove any cleaning chemical or residue. Position the battery to avoid water from pooling near the terminals. 5. Dry thoroughly before you insert the battery into the product or charger. 6507-009-001 Rev AB.3 59 EN PPrreevveennttiivvee mmaaiinntteennaannccee WWAARRNNIINNGG -- Do not use bare hands to check for hydraulic leaks. CCAAUUTTIIOONN -- Always use authorized parts to avoid the risk of product damage. Establish and follow a maintenance schedule and keep records of the maintenance activity. Remove product from service before you perform the preventive maintenance inspection. You may need to perform preventive maintenance checks more often based on your level of product usage. Service only by qualified personnel. When using maintenance products, follow the directions of the manufacturer and reference all Material Safety Data Sheets

(MSDS). LLuubbrriiccaattiioonn CCAAUUTTIIOONN -- Do not lubricate the bearings in the X-frame as it will degrade the performance of the cot and may void its warranty. The cot has been designed to operate without the need for lubrication. RReegguullaarr iinnssppeeccttiioonn aanndd aaddjjuussttmmeennttss The following schedule is a general guide to maintenance. Factors such as weather, terrain, geographical location, and individual usage will alter the required maintenance schedule. If you are unsure how to perform these checks, contact your Stryker service technician. If you are in doubt as to what intervals to follow to maintain your product, consult your Stryker service technician. Check each routine and replace worn parts if necessary. EEvveerryy mmoonntthh oorr ttwwoo hhoouurrss Inspect these items every month or two hours, whichever comes first. IItteemm Settings Cylinder Cables and wires IInnssppeecctt In-fastener shutoff configuration Extend cylinder rod and wipe with a soft cloth and household cleaner No hanging wires from routings or connections Hand tighten foot end electronics cable Manual back-up release handle Manual back-up release handle functions Litter Base Wheels Head section Foot section Restraint Frame and litter Frame and base All wheels are secure, roll, and swivel Pull toward the head section to check that the safety bar swings and rotates freely and pulls back to the home position Extend and retract Functions and latches Function with no excessive wear (such as a bent or broken receiver or latch plate or torn or frayed webbing) EN 60 6507-009-001 Rev AB.3 IItteemm Battery Charger IInnssppeecctt Housing and terminal area for cracks or damage before first and every use For cuts in the cord, bent pins or contacts, or cracks in the housing before first and every use EEvveerryy tthhrreeee mmoonntthhss oorr ssiixx hhoouurrss Inspect these items every three months or six hours, whichever comes first. IItteemm Hydraulics IInnssppeecctt Motor mount fasteners are secure No hydraulic fluid leaks No leaks from reservoir Cables and wires No damage or pinching of wiring harness, cable, or lines Manual back-up release handle Litter Base X-frame Head section Foot section No damaged connectors Base extends and retracts when you pull the manual back-

up release handle Cot does not lower when you pull the manual backup release handle with 125 lb (57 kg) or more on the cot All fasteners are secure Backrest cylinder operates Adjust pneumatic cylinder for full range of motion, if required All fasteners are secure X-frame expands and retracts All fasteners are secure Head section extends and locks Transport handle extends and locks in 90 degree upright position All fasteners are secure Foot section extends and locks in the retracted, mid, and extended positions Stow and lock transport handle Foot end guide lights operate Accessories and parts (optional) All accessories and parts operate 6507-009-001 Rev AB.3 61 EN EEvveerryy ssiixx mmoonntthhss oorr 1122 hhoouurrss Inspect these items every six months or 12 hours, whichever comes first. IItteemm Electronic controls/functions Switches Litter Mattress Base Wheels Head section Foot section IInnssppeecctt Extend cot to raised position, measure and check load height Jog function operates High speed retract and extend operates Bumper detection operates Press the release or transport height button and confirm correct height Measure load height and confirm correct height No damage or wear to the switches All switches operate No bent, broken, or damaged components No damage or tears on cot grips Siderails operate and latch Footrest operates No cracks or tears No bent, broken, or damaged components Cot retaining post is secure. If not, replace the screw. No excessive damage to X-frame guards Free of debris SStteeeerr--LLoocckk and wheel locks operate Check brake cable (between SStteeeerr--LLoocckk and wheel lock) for wear, bends, creases No bent, broken, or damaged components Grip bar has no excessive damage or tears Load wheels are secure and roll No bent, broken, or damaged components Grip bar has no excessive damage or tears EEvveerryy 1122 mmoonntthhss oorr 2244 hhoouurrss Inspect these items every 12 months or 24 hours, whichever comes first. IItteemm Settings EN 62 IInnssppeecctt Cot and fastener fit and function Safety bar connects to the vehicle safety hook 6507-009-001 Rev AB.3 IItteemm IInnssppeecctt Manual back-up release handle Returns to the stowed position Litter Base All welds are intact, not cracked, or broken Warning labels present and legible All welds are intact, not cracked, or broken Retractable head section oxygen bottle holder (optional) Straps and clips for wear Foot section Cables and wires Foot end hitch latch hooks not worn Foot end interface board (FEIB) cable connector is tight 6507-009-001 Rev AB.3 63 EN WWiirreelleessss nnoottiiffiiccaattiioonnss For product equipped with optional wireless communication technology, these statements apply to the countries as indicated:

CCoouunnttrryy NNoottiiffiiccaattiioonn Contains IC: 4919E-SDMACP Contains IC: 4919E-6507 Canada This device complies with Innovation, Science and Economic Development Canadas license-

exempt RSSs. Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. Le prsent appareil est conforme aux CNR d'Industrie Canada applicables aux appareils radio exempts de licence. L'exploitation est autorise aux deux conditions suivantes : (1) l'appareil ne doit pas produire de brouillage, et (2) l'utilisateur de l'appareil doit accepter tout brouillage radiolectrique subi, mme si le brouillage est susceptible d'en compromettre le fonctionnement. Mexico La operacin de este equipo est sujeta a las siguientes dos condiciones: (1) es posible que este equipo o dispositivo no cause interferencia perjudicial y (2) este equipo o dispositivo debe aceptar cualquier interferencia, incluyendo la que pueda causar su operacin no deseada. Contains FCC ID: Z7A-SDMACP Contains FCC ID: Z7A-6507 United States This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Changes or modifications not expressly approved by the party responsible for compliance could void the users authority to operate the equipment. Frequency Tolerance: +/-20 ppm WWiirreelleessss ccooeexxiisstteennccee nnoottiiffiiccaattiioonnss Microwaves are regulated by the federal government through 21 CFR 1030.10 such that the amount of power that can leak from a microwave oven over its lifetime is very small, such as 5mW/cmsq @ 2 from the plane of the microwave surface. This radiation will roll off rapidly as the distance between the microwave and the measurement point increases. Other radiation in this band can be generated from unintentional radiators and from the control and source circuity in the microwave. The level of this radiation is also controlled via federal regulations from the FCC and is not of a high magnitude. These two sources of noise are both contained inside the microwave oven which is shielded and designed to minimize this radiation. In general, the user of the medical device will not be in close proximity to the microwave oven when using the medical device. EN 64 6507-009-001 Rev AB.3 EEMMCC iinnffoorrmmaattiioonn WWAARRNNIINNGG Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be used no closer than 12 inches (30 cm) to any part of PPoowweerr--PPRROO 2, including cables specified by the manufacturer. Avoid stacking or placing other equipment adjacent to PPoowweerr--PPRROO 2 to prevent improper operation of the products. If such use is necessary, carefully observe the cot and the other equipment to verify proper operation. The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation. GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc eemmiissssiioonnss EEmmiissssiioonnss tteesstt CCoommpplliiaannccee EElleeccttrroommaaggnneettiicc eennvviirroonnmmeenntt PPoowweerr--PPRROO 2 is intended for use in the electromagnetic environment specified below. The customer or the user of PPoowweerr--PPRROO 2 should assure that they are used in such an environment. RF emissions CISPR 11 RF emissions CISPR 11 RF emissions CISPR 11 Group 2 Group 1 Class B PPoowweerr--PPRROO 2 with the PPoowweerr--LLOOAADD compatibility option must emit electromagnetic energy in order to perform its intended function. Nearby electronic equipment may be affected. The emissions characteristics of this equipment make it suitable for use in professional healthcare facilities, emergency medical services, and home healthcare environments. If it is used in other environments, this equipment might not offer adequate protection to radio-frequency communication services and power supply networks. The user might need to take mitigation measures, such as relocating or reorienting the equipment. GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc iimmmmuunniittyy PPoowweerr--PPRROO 2 is suitable for use in a professional healthcare facility, home, and EMS environments. PPoowweerr--PPRROO 2 is not suitable for use in environments exceeding immunity test conditions that the product was evaluated to, such as near high frequency (HF) surgical equipment and inside of the radio frequency (RF) shielded room of magnetic resonance imaging (MRI) equipment. The customer or the user of PPoowweerr--PPRROO 2 should assure that it is used in such an environment and that the electromagnetic environment guidance listed below is followed. IImmmmuunniittyy tteesstt IIEECC 6600660011 tteesstt lleevveell CCoommpplliiaannccee lleevveell Electrostatic discharge

(ESD) IEC 61000-4-2

+8 kV contact

+8 kV contact

+15 kV air

+15 kV air Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 30 A/m 30 A/m EElleeccttrroommaaggnneettiicc eennvviirroonnmmeenntt--gguuiiddaannccee Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. 6507-009-001 Rev AB.3 65 EN GGuuiiddaannccee aanndd mmaannuuffaaccttuurreerrss ddeeccllaarraattiioonn -- eelleeccttrroommaaggnneettiicc iimmmmuunniittyy Radiated RF 10 V/m IEC 61000-4-3 80 MHz to 2.7 GHz 10 V/m Portable and mobile RF communications equipment should follow the guidance in the table titled Recommended separation distances between portable and mobile RF communication equipment and PPoowweerr--PPRROO 2. If the mobile service is not listed in the table, the recommended separation distance should be calculated from the equation appropriate for the frequency of the transmitter. Recommended separation distance:

D=(0.6) (P) where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol:

NNoottee -- These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which PPoowweerr--PPRROO 2 is used exceeds the applicable RF If abnormal compliance level above, performance is observed, additional measures may be necessary, such as reorienting or relocating PPoowweerr--PPRROO 2. the PPoowweerr--PPRROO 2 system should be observed to verify normal operation. b Over the frequency range 150 kHz to 80 MHz, field strengths are less than 10 V/m. EN 66 6507-009-001 Rev AB.3 RReeccoommmmeennddeedd sseeppaarraattiioonn ddiissttaanncceess bbeettwweeeenn ppoorrttaabbllee aanndd mmoobbiillee RRFF ccoommmmuunniiccaattiioonnss eeqquuiippmmeenntt aanndd PPoowweerr--

PPRROO 22 BBaanndd ((MMHHzz)) SSeerrvviiccee MMaaxxiimmuumm ppoowweerr

((WW)) MMiinniimmuumm sseeppaarraattiioonn ddiissttaannccee

((mm)) PPoowweerr--PPRROO 2 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of PPoowweerr--PPRROO 2 can help prevent electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters), PPoowweerr--PPRROO 2, and cables, as recommended below, according to the maximum output power of the communications equipment. 380-390 430-470 704-787 800-960 1,700-1,990 2,400-2,570 5,100-5,800 TETRA 400 GMRS 460 FRS 460 LTE band 13, 17 GSM 800/900 TETRA 800 iDEN 820 CDMA 850 LTE band 5 GSM 1800 CDMA 1900 GSM 1900 DECT LTE band 1, 3, 4, 25 UMTS Bluetooth WLAN 802.11 b/g/n RFID 2450 LTE band 7 WLAN 802.11 a/n 1.8 2.0 0.2 2.0 0.3 0.3 0.3 0.3 2.0 0.3 2.0 0.2 0.3 0.3 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters

(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NNoottee: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. 6507-009-001 Rev AB.3 67 EN CCAAUUTTIIOONN -- Changes or modifications to the AAllvvaarriiuumm Battery Management System, not expressly approved by Stryker, could void the user's authority to operate the equipment. FFoorr UUnniitteedd SSttaatteess oonnllyy::

AAllvvaarriiuumm BBaatttteerryy MMaannaaggeemmeenntt SSyysstteemm:: MMooddeell 665500770000008800330011 ((bbaatttteerryy)) aanndd MMooddeell 665500770000445500330011 ((cchhaarrggeerr)) NNoottee -- This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

Reorient or relocate the receiving antenna Increase the separation between the equipment and receiver Connect the equipment into an outlet on a circuit different from that to which the receiver is connected Consult the dealer or an experienced radio or TV technician for help EN 68 6507-009-001 Rev AB.3 Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA 6507-009-001 Rev AB.3 WCR: AD.16 2021-08

Page: 1 of 4 Internal View of EUT Antenna-1 Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd. Page: 2 of 4 Antenna-2 Antenna-3 Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd. Page: 3 of 4 Antenna-4 Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd. Page: 4 of 4 Antennal Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd.

Page: 1 of 2 PHOTOGRAPHS OF EUT All View of EUT Front View of EUT Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd. Page: 2 of 2 Back View of EUT Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only. 90 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for elec-

tronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Companys findings at the time of its intervention only and within the limits of Clients instructions, if any. The Companys sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or ap-

pearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. No.134,WuKungRoad,NewTaipeiIndustrialPark,WukuDistrict,NewTaipeiCity,Taiwan24803/ 134 www.tw.sgs.com Member of SGS Group t (886-2) 2299-3279 f (886-2) 2298-0488 SGS Taiwan Ltd.

Specification/Spec Label Content and Location:

Serial Number Labels Content and Location:

Label 1 Content and Location:

Label 2 Content and Location:

Overall Label Locations:

Serial Number Label Spec Label Label 1 Label 2

Date: July 27, 2021 UL LLC 12 Laboratory Dr RTP, NC 27709, USA To whom it may concern:

I, the undersigned, hereby authorize UL LLC to act on our behalf in all manners relating to application for equipment authorization, including signing of all documents relating to these matters. Any and all acts carried out by UL LLC on our behalf shall have the same effect as acts of our own. I, the undersigned, hereby certify that we are not subject to a denial of federal benefits, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). In authorizing UL LLC as our agent, we still recognize that we are responsible to:

a) b) c) d) e) f) g) h) comply with the relevant provisions of the certification program;

make all necessary arrangements for the conduct of the evaluation, including provision for examining documentation and access to all areas, records (including internal audit reports) and personnel for the purposes of evaluation (e.g. testing, inspection, assessment, surveillance, reassessment) and resolution of complaints;

make claims regarding certification only in respect of the scope for which certification has been granted;

do not use our product certification in such a manner as to bring UL LLC into disrepute and not make any statement regarding our product certification which UL LLC may consider misleading or unauthorized;

upon suspension or cancellation of certification, discontinue use of all advertising matter that contains any reference thereto and return any certification documents as required by UL LLC;

use certification only to indicate the products are certified as being in conformity with specified standards;

endeavor to ensure that no certificate or report nor any part thereof is used in a misleading manner;

ensure that any reference to our product certification in communication media such as documents, brochures or advertising, complies with the requirements of UL LLC;

i) j) keep a record of all complaints made known to the us relating to the products compliance with requirements of the relevant standard and to make these records available to UL LLC when requested;

take appropriate action with respect to such complaints and any deficiencies found in products or services that affect compliance with the requirements for certification;

k) document the actions taken. This authorization is valid until further written notice from the applicant. Sincerely Yours, Divya Murali Director, Global Regulatory Affairs Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 567 8254

stryker October 8, 2019 AUTHORIZATION LETTER To whom it may concern:

thereby authorize Divya Murali Regulatory Affairs Manager at Stryker Medical, to act on behalf of Stryker Medical in all matters relating to the FCC grantee activities of inquiries and application for equipment authorization in connection with FCC FRN 0021243142, including signing of all documents relating to these matters. If you have any questions regarding this authorization, please do not hesitate to contact me. Sincerely yours, Mike Hayes Senior Principal Engineer EE Stryker Medical 3800 E. Centre Ave., Portage, MI 49002 Tel: (269) 389 6754 Email: mike.haves@stryker.com 3800 E. Centre Ave., Portage, MI 49002 USA | P +1 269 329 2100 | stryker.com

July 27, 2021 Federal Communications Commission 7435 Oakland Mills Road Columbia MD 21046 Subject: Request for Confidentiality FCC ID: Z7A-SDMACP To Whom It May Concern:

Pursuant to the provisions of Sections 0.457 and 0.459 of the Commissions rules (47 CFR 0.457, 0.459), we are requesting the Commission to withhold the following attachments as confidential document from public disclosure indefinitely. Engineering Drawings/Specifications Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. In additional to above mentioned documents, pursuant to Public Notice DA 04-1705 of the Commissions policy, in order to comply with the marketing regulations in 47 CFR 2.803 and the importation rules in 47 CFR 2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices. We are requesting the commission to grant short-term confidentiality request on the following attachments until 180 days after the grant date:

Internal Photos It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and that information will be available for public review once the grant of equipment authorization is issued. Best Regards, Divya Murali Director, Global Regulatory Affairs Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 567 8254

FCC Class II Permissive Change Request Letter Date: September 7, 2021 To Federal Communications Commission:

RE: FCC Permissive II Change Request for Company: Stryker Medical FCC ID: Z7A-SDMACP We are submitting an application for a class II permissive change to the FCC approval of the Company name:

Stryker Medical, product description: Embedded wireless module (FCC ID: Z7A-SDMACP, Original Grant Date:

10/29/2019). The transmitter module itself has not changed. The antenna and rated power have also not changed. Here are the changes:

Add SAR (portable condition) to the Silex SX-SDMAC-2832S+ module for Stryker Medical Ambulance Cot Power-PRO 2 (Models 650700000000, 650705550001, 650705550002, and 650705550003). The Bluetooth transmitter for FCC ID: Z7A-SDMACP is disabled while used with Stryker Medical Ambulance Cot Power-PRO 2 (Models 650700000000, 650705550001, 650705550002, and 650705550003). Sincerely, Divya Murali Director, Global Regulatory Affairs Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 389 6998

Date: May 8, 2020 UL LLC 12 Laboratory Dr RTP, NC 27709, USA To whom it may concern:

I, the undersigned, hereby authorize UL LLC to act on our behalf in all manners relating to application for equipment authorization, including signing of all documents relating to these matters. Any and all acts carried out by UL LLC on our behalf shall have the same effect as acts of our own. I, the undersigned, hereby certify that we are not subject to a denial of federal benefits, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). In authorizing UL LLC as our agent, we still recognize that we are responsible to:

a) b) c) d) e) f) g) h) comply with the relevant provisions of the certification program;

make all necessary arrangements for the conduct of the evaluation, including provision for examining documentation and access to all areas, records (including internal audit reports) and personnel for the purposes of evaluation (e.g. testing, inspection, assessment, surveillance, reassessment) and resolution of complaints;

make claims regarding certification only in respect of the scope for which certification has been granted;

do not use our product certification in such a manner as to bring UL LLC into disrepute and not make any statement regarding our product certification which UL LLC may consider misleading or unauthorized;

upon suspension or cancellation of certification, discontinue use of all advertising matter that contains any reference thereto and return any certification documents as required by UL LLC;

use certification only to indicate the products are certified as being in conformity with specified standards;

endeavor to ensure that no certificate or report nor any part thereof is used in a misleading manner;

ensure that any reference to our product certification in communication media such as documents, brochures or advertising, complies with the requirements of UL LLC;

i) j) keep a record of all complaints made known to the us relating to the products compliance with requirements of the relevant standard and to make these records available to UL LLC when requested;

take appropriate action with respect to such complaints and any deficiencies found in products or services that affect compliance with the requirements for certification;

k) document the actions taken. This authorization is valid until further written notice from the applicant. Sincerely Yours, Divya Murali Sr. Regulatory Affairs Manager Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 389 6998

June 2, 2020 Federal Communications Commission 7435 Oakland Mills Road Columbia MD 21046 Subject: Request for Confidentiality FCC ID: Z7A-SDMACP To Whom It May Concern:

Pursuant to the provisions of Sections 0.457 and 0.459 of the Commissions rules (47 CFR 0.457, 0.459), we are requesting the Commission to withhold the following attachments as confidential document from public disclosure indefinitely. Engineering Drawings/Specifications Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. In additional to above mentioned documents, pursuant to Public Notice DA 04-1705 of the Commissions policy, in order to comply with the marketing regulations in 47 CFR 2.803 and the importation rules in 47 CFR 2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices. We are requesting the commission to grant short-term confidentiality request on the following attachments until 180 days after the grant date:

External Photos Internal Photos Test Setup Photos User Manual It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and that information will be available for public review once the grant of equipment authorization is issued. Best Regards, Divya Murali Regulatory Affairs Manager Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 389 6998

FCC Class II Permissive Change Request Letter Date: May 27, 2020 To Federal Communications Commission:

RE: FCC Permissive II Change Request for Company: Stryker Medical FCC ID: Z7A-SDMACP We are submitting an application for a class II permissive change to the FCC approval of the Company name:

Stryker Medical, product description: Embedded wireless module (FCC ID: Z7A-SDMACP, Original Grant Date:

10/29/2019). The transmitter module itself has not changed. The antenna and rated power have also not changed. Here are the changes:

Add SAR (portable condition) to the Silex SX-SDMAC-2832S+ module for Stryker Medical Bed Procuity (Model 3009). The Bluetooth transmitter for FCC ID: Z7A-SDMACP is disabled while used with Stryker Medical Bed Procuity

(Model 3009). Stryker Medical Bed Procuity (Model 3009) contains Bluetooth transmitter FCC ID: QOQW32I. Sincerely, Divya Murali Regulatory Affairs Manager Divya.Murali@stryker.com Medical 3800 E. Centre Avenue, Portage, MI 49002 USA P +1 269 389 6998