FCC ID: SXEEMUIP2213RF LCD USER INTERFACE

MUIP-2213 13.3 LCD User Interface User Guide ENABLING BRIGHT OUTCOMES Barco NV Beneluxpark 21, 8500 Kortrijk, Belgium www.barco.com/en/support www.barco.com Registered office: Barco NV President Kennedypark 35, 8500 Kortrijk, Belgium www.barco.com/en/support www.barco.com Table of contents 1 Welcome! ........................................................................................................................ 5 1.1 What's in the box ............................................................................................................................... 6 Product overview. ............................................................................................................................. 6 1.2 2 Installation ....................................................................................................................... 9 Cable connections ........................................................................................................................... 10 2.1 Cable routing ................................................................................................................................... 11 2.2 Desktop support installation (optional). .......................................................................................... 12 2.3 3 Maintenance ................................................................................................................. 15 Scheduled maintenance .................................................................................................................. 16 Cleaning .......................................................................................................................................... 16 3.1 3.2 4 Important information .................................................................................................... 17 Safety information ........................................................................................................................... 18 4.1 Cybersecurity .................................................................................................................................. 21 4.2 Environmental information ............................................................................................................... 21 4.3 Biological hazard and returns Decommissioning .......................................................................... 23 4.4 Regulatory information .................................................................................................................... 24 4.5 EMC notice ...................................................................................................................................... 24 4.6 Explanation of symbols.................................................................................................................... 27 4.7 Legal disclaimer............................................................................................................................... 30 4.8 Technical specifications ................................................................................................................... 31 4.9 K5902132 (451920612535) /04 MUIP-2213 3 4 K5902132 (451920612535) /04 MUIP-2213 Welcome!

1 Warnings, cautions, notes and tips There are four levels of precautionary or advisory statements that may be used in this user guide. In descending order of importance, they are:

WARNING: Describes hazards or dangers that might result in personal injury or death. CAUTION: Describes hazards that could damage the product. Gives additional information about the described subject. Gives extra advice about the described subject. K5902132 (451920612535) /04 MUIP-2213 5 Welcome!

1.1 What's in the box Overview MUIP-2213 13.3 Computing Touchscreen Module Power cord provided according to final country destination; not provided for the configuration without power supply. 1x printed User Guide (English) Keep your original packaging. It is designed for this display and is the ideal protection during transport and storage. 1.2 Product overview Front Image 11 1. MUIP-2213 2. Power Button:

Push short to turn the equipment ON/OFF. 3. Desktop support (optional) 6 K5902132 (451920612535) /04 MUIP-2213 Welcome!

Back Welcome!

Image 12 Rear cover fixation screw holes (2x) Rear cover (standard open / optional closed version) 1 x USB 3.0 port Type A connector Gigabit Ethernet Connector (LAN1) Gigabit Ethernet Connector (LAN2) Power jack input connector VESA 75 mm mounting screw holes (4x), its applicable for desk, not wall using. 8 K5902132 (451920612535) /04 MUIP-2213 Installation 2 WARNING: Read all the important safety information before installing and operating your monitor. Please refer to the dedicated chapter in this user guide. WARNING: Sufficient expertise is required to install this equipment. All devices and complete setup must be tested before taking into operation. CAUTION: When the display is assembled in the medical system, take care of the fixation of all cables, to avoid unwanted detachment. CAUTION: The equipment is not intended to be sterilized. K5902132 (451920612535) /04 MUIP-2213 9 Installation 2.1 Cable connections Opening and closing the rear cover 1. Remove the two rubber-caps which cover the fixation screws. 2. Remove the two fixation screws and remove the rear cover from the MUIP-2213. Image 21 3. To properly close the rear cover, first route the cables as described in Cable routing, page 11. Install the rear cover and follow the above steps in reverse order. Power and LAN connection The MUIP-2213 Computing Touch-Screen Module working as an intelligent User-Interface is usually connected to the system via Ethernet LAN connection and / or USB interface connection. 1. Connect the power connector to the power jack input. Image 22 2. Connect the LAN connector to the LAN input. Image 23 10 K5902132 (451920612535) /04 MUIP-2213 Other cable connections example (open rear cover version only) 1. Connect the USB 3.0 connector to the USB 3.0 input. Installation Image 24 2.2 Cable routing Open rear cover version The cables can be routed in two different ways:

1. Route the cables straight downwards (as shown below). Image 25 2. Route the cables behind the pin (as shown below). K5902132 (451920612535) /04 MUIP-2213 11 Installation Image 26 This routing can only be performed if maximum 3 cables are installed. Closed rear cover version (optional) 1. The closed rear cover (2) provided hereby, allows routing of all connecting cables through its square hole, instead of routing them straight downwards. 2.3 Desktop support installation (optional) Orientation A desktop support may be included in the MUIP-2213 package. This support can be installed in two different orientations, allowing to achieve a different angle of the display. 12 K5902132 (451920612535) /04 MUIP-2213 Installation Image 28 Installation 1. Place the desktop support in the desired orientation. 2. Install the MUIP-2213 on the desktop support in landscape orientation. 3. Install and tighten the four VESA 75 mm mounting screws. Image 29 K5902132 (451920612535) /04 MUIP-2213 13 Installation Image 210 14 K5902132 (451920612535) /04 MUIP-2213 Maintenance 3 K5902132 (451920612535) /04 MUIP-2213 15 Maintenance 3.1 Scheduled maintenance About The MUIP-2213 does not require any scheduled maintenance or calibration activities. In case of inconsistencies, please contact Barco Healthcare. 3.2 Cleaning WARNING: Unplug the power cable from the mains power input before cleaning the display. CAUTION: Take care not to damage or scratch the front glass or LCD. Be careful with rings or other jewelry and do not apply excessive pressure on the front glass or LCD. CAUTION: Do not apply or spray liquid directly to the display as excess liquid may cause damage to internal electronics. Instead, apply the liquid to a cleaning cloth. To clean the display Clean the display using a sponge, cleaning cloth or soft tissue, lightly moistened with a recognized cleaning product for medical equipment. Read and follow all label instructions on the cleaning product. In case of doubt about a certain cleaning product, use plain water. Possible cleaning solutions:

75% isopropyl alcohol 1.6% aqueous ammonia Sodium hypochlorite (bleach) 5%

0.5% Chlorehexidine in 70% isopropyl alcohol Do not use following products:

Alcohol/solvents at higher concentration > 70%

Strong alkalis lye, strong solvents Acid Detergents with fluoride Detergents with ammonia at higher concentration > 1.6%

Detergents with abrasives Steel wool Sponge with abrasives Steel blades Cloth with steel thread 16 K5902132 (451920612535) /04 MUIP-

21122213 Important information 4 K5902132 (451920612535) /04 MUIP-2213 17 Important information 4.1 Safety information General recommendations Read the safety and operating instructions before operating the device. Retain safety and operating instructions for future reference. Adhere to all warnings on the device and in the operating instructions manual. Follow all instructions for operation and use. Electrical Shock or Fire Hazard To prevent electric shock or fire hazard, do not remove cover. No serviceable parts inside. Refer servicing to qualified personnel. Do not expose this apparatus to rain or moisture. Modifications to the unit Do not modify this equipment without authorization of the manufacturer. Preventive maintenance Periodic maintenance inspections are essential to keep the monitor in optimum condition and ensure safe operation. With the monitor disconnected from the mains, perform the following periodic check:

Check the integrity of the power cord and inspect its routing, so that it is not under the risk of being punched or cut. General recommendations: Keep the monitor clean to prolong its operational lifetime. LCD panel performance may deteriorate in the long term. Periodically check that it is correctly operating. Periodically check the tightness of the VESA mount screws. If not sufficiently tight, the monitor may detach from the arm, which may result in injury or equipment damage. Type of protection (electrical):

Monitor provided with external power supply: Class II equipment. Monitor provided without external power supply: Class I or II, depending from the Class of the external power supply used. Degree of safety (flammable anesthetic mixture):

Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. The equipment is not operable if the air oxygen content is above 25%. Non-patient care equipment Equipment primarily for use in a health care facility that is intended for use where contact with a patient is unlikely (no applied part) The equipment should not be used with life support equipment. The user should not touch the signal input ports (SIP) / signal output ports (SOP) and the patient at the same time. The rear cover must be kept closed and screwed. Child safety Equipment not suitable for use in locations where children are likely to be present. Mission critical applications We strongly recommend to immediately have a replacement display available in mission critical applications. Use of electrical surgical knives Provide as much distance as possible between the electrosurgical generator and other electronic equipment

(such as monitors). An activated electrosurgical generator may cause interference with this equipment and can disrupt the functionality of the display. 18 Power connection (the configuration without power supply) Important information Power requirements: The equipment must be powered using medical approved AC/DC power supply . The medical approved AC/DC power supply must be powered by the AC mains voltage. The power supply is specified as a part of the ME equipment or combination is specified as an ME system. The equipment should be installed near an easily accessible wall socket. To disconnect the main power, unplug the AC adapter. The equipment is intended for continuous operation. The compliance of the equipment with the Medical Safety and EMC requirements has been evaluated with the provided medical grade power supply. If a different power supply is used, further investigation for Safety and EMC requirements have to be performed at system level. Do not use the supplied AC adapter for powering other devices. Do not move the equipment while the power cord and connection cables are connected. Otherwise, damage to the equipment, power cord and connection cables, fire or an electric shock may result. Power connection Used in conjunction with a 19V power supply

(CINCON ELECTRONICS CO LTD, type TR60M19) Power requirements: The equipment must only be powered using the delivered medical approved 19VDC

) SELV power supply. The medical approved DC (

) power supply must be powered by the AC mains voltage. The power supply is specified as a part of the ME equipment or combination is specified as a ME system. To avoid the risk of electric shock, this equipment must only be connected to a supply mains The equipment should be installed near an easily accessible outlet. The equipment is intended for continuous operation. Power connection Equipment with external 12V-24 VDC power supply. Power requirements: The equipment must only be powered using the delivered medical approved 12-24 VDC (

)SELV power supply. The medical approved DC(

) power supply must be powered by the AC mains voltage. The power supply is specified as a part of the ME equipment or combination is specified as a ME system. To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth. The equipment should be installed near an easily accessible outlet. The equipment is intended for continuous operation. If a different power supply will be used, further investigation for safety and EMC requirements have to be performed at system level. 19 Important information Transient over-voltage To fully disengage the power from the device, please disconnect the power cord from the AC inlet. Connections Any external connection with other peripherals must follow the requirements of clause 16 of IEC60601-1 3.2rd. Ed. or Table BBB.201 of IEC 60601-1-1 for the medical electrical systems. To maintain compliance with EMC Regulation, use only shielded interface cables for the connection to peripheral devices. Power cords:

Please use the power cord provided with this equipment. If a power cord is not supplied with this equipment, please contact your supplier. For all other cases, please use a power cord that matches the AC voltage of the power outlet and has been approved by and complies with the safety standard of your particular country. Do not overload wall sockets and extension cords as this may result in fire or electric shock. Mains lead protection: Power cords should be routed so that they are not likely to be walked upon or pinched by items placed upon or against them, paying particular attention to cords at plugs and receptacles. The power supply cord should be replaced by the designated operator only, at all time. Liquids and moisture Never expose the equipment to liquids or moisture. Never use the equipment near water - e.g. near a bathtub, washbasin, swimming pool, kitchen sink, laundry tub or in a wet basement. To check IP rate, please refer to product label or the table of specification. The equipment is IPx3 compliant. Power supply is IPx0 ( when provided) Moisture condensation Do not use the equipment under rapidly changing temperature and humidity conditions or avoid direct contact with cold air from air-conditioning outlet. Moisture may condense on the surface or inside of the equipment, or create a mist residue inside the protection plate. This is not a malfunction of the product itself, although it may cause damage to the equipment. If condensation exists, leave the equipment unplugged until there is no condensation. Ventilation When installing the device in a cupboard or another enclosed location, heed the necessary space between the set and the sides of the cupboard. The LCD panel becomes warm during operation. This is not a malfunction. Allow adequate air circulation to reduce the temperature of the equipment. Installation Place the equipment on a flat, solid and stable surface that can support the weight of at least 3 units. If you use an unstable cart or stand, the equipment may fall, causing serious injury to a child or adult and/or serious damage to the equipment. Do not allow to climb or rest on the equipment. When the equipment is attached to an arm, do not use the equipment as a handle or grip in order to move the equipment. Please refer to the instruction manual of the arm for instructions on how to move the arm with the equipment. Provide full attention to safety during installation, periodic maintenance and examination of this equipment. Sufficient expertise is required for installing this equipmentt. Be sure to entrust the attachment of this 20 Important information equipment to the wall to a duly skilled technician and pay adequate attention to safety during the installation and usage. The manufacturer is not liable for any damage or injury caused by mishandling or improper installation. When the display is assembled in the medical system, take care of unwanted detachment. The equipment should be installed near an easily accessible place. Do not install or leave the unit in places subject to extreme temperatures, near a radiator, heating vent, or in places subject to mechanical vibration or shock. Subjecting the LCD display to extreme temperatures, could cause deformations of the casing or malfunctions. Avoid to place the unit near any equipment that generates a strong electro-magnetic field, such as surgical knife but also other medical appliances. Avoid places subject to inordinate amounts of dust, dirt, or sand, for example near an open window or an outdoor exit. If setting up temporarily in an outdoor environment, be sure to take adequate precautions against airborne dust and dirt. Otherwise unrecoverable malfunctions could occur. Handling Do not press on or scratch the front protection screen. Do not place a heavy object on the equipment. If the equipment is used in a cold place, a residual image may appear in the screen. This is not a malfunction. The screen returns to normal as the temperature rises to a normal operating level. If a still picture is displayed for a long time, a residual image may appear for a while. The residual image will eventually disappear. Transportation Disconnect the cable from the equipment when transporting. When you transport the equipment, hold it firmly in both hands. If you drop the equipment, you may be injured or the equipment may be damaged. When you transport the equipment for repair or shipment, use the original cardboard box and packing materials. Batteries The internal battery is foreseen mainly for preventing the operative-system from crash in case of momentary drop of the mains power. The internal battery capacity could maintain the unit to work for a time of about one hour maximum. This device uses an RTC battery (Mod. CR-2032) and a Lithium Ion battery pack (Mod. RRC2130 ). RTC battery (Mod. CR-2032), normal voltage: 3V. normal capacity: 220mAh. Lithium Ion battery pack (Mod. RRC2130), normal voltage: 7.2V. normal capacity: 4.17Ah. Both batteries are not user-replaceable. Do not attempt to replace them, contact Barco authorized repair facilities. Batteries used with this equipment have been tested for compatibility and should only be replaced with approved parts. The batteries are not designed to be charged by any other electrical source. Charging could generate gas and internal short-circuiting, leading to distortion, leakage, overheating, explosion, or fire. CAUTION: Risk of Explosion if Battery is replaced by an Incorrect Type. Dispose of Used Batteries According to the Instructions Connection of PEMS by network/data coupling to other equipment Connection of the PEMS to a network/data coupling that includes other equipment could result in previously unidentified risks to patients, operators or third parties. The responsible organization should identify, analyze, evaluate and control these risks. Subsequent changes to the network/data coupling could introduce new RISKS and require additional analysis. Changes to the NETWORK/DATA COUPLING include:

- Changes in NETWORK/DATA COUPLING configuration;

- Connection of additional items to the NETWORK/DATA COUPLING;

- Disconnecting items from the NETWORK/DATA COUPLING;

21 Important information

- Update of equipment connected to the NETWORK/DATA COUPLING;

- Upgrade of equipment connected to the NETWORK/DATA COUPLING. Malfunctions Disconnect the equipments power cord from the AC inlet and refer servicing to qualified service technicians under the following conditions:

If the power cord or plug is damaged or frayed. If liquid has been spilled into the equipment. If the equipment has been exposed to rain or water. If the equipment does not operate normally when the operating instructions are followed. Adjust only those controls that are covered by the operating instructions since improper adjustment of other controls may result in damage and will often require extensive work by a qualified technician to restore the product to normal operation. If the equipment has been dropped or the cabinet has been damaged. If the product exhibits a distinct change in performance, indicating a need for service General warnings All devices and complete setup must be tested and validated before taking into operation. At end user application level, it is necessary to foresee a backup unit in case the equipment fails. The enclosure has to be checked upon collision damage; refer to qualified service personnel. The monitor is intended for indoor use The monitor is not intended to be sterilized The monitor has not applied parts, but the front side of the LCD panel and the plastic enclosure have been treated as applied part because considered accidentally touchable by the patient for a time <1 minute. Do not connect to the internet before you have installed an anti-virus software and Internet firewall to protect the Barco User Interface from viruses. National Scandinavian Deviations for CL. 1.7.2 Finland: "Laite on liitettv suojamaadoituskoskettimilla varustettuun pistorasiaan"

Norway: "Apparatet m tilkoples jordet stikkontakt"

Sweden: "Apparaten skall anslutas till jordat uttag"

CAUTION: If the MUIP-2213 is integrated as component in a medical-equipment providing life-

support, the user-integrator shall provide the necessary precautions to avoid possible damage, injury or harm to the patients. The MUIP-2213 has no essential performances and the provided Windows OS is not a class-A software. CAUTION: The enclosure has to be checked upon collision damage, refer to qualified service personnel. 4.2 Cybersecurity Hospital IT security To prevent unauthorized access to the device, the organization incorporating the MUIP-2213 in their IT network shall have the necessary state-of-the-art policies, processes, standards and other security measures in place to incorporate, support and protect the device into the IT network. This shall include the application of risk management (e.g. by following IEC 80001-1:2010 or equivalent standards). To ensure optimal security of your device, we strongly recommend following these essential 22 cybersecurity measures:

Important information Upon initial logon, change the password for the service account. This helps mitigate potential vulnerabilities and unauthorized access to your system. Enable the TPM feature (in the BIOS) off your device. TPM provides hardware-based security capabilities, such as cryptographic key generation and storage, that significantly enhance the protection of sensitive data. Activate the BitLocker encryption feature, which safeguards your data by encrypting the entire hard drive. BitLocker prevents unauthorized access to data in case of theft or unauthorized physical access to the device. Activate the Secure Boot or Device Guard feature, when feasible, to ensure that only trusted and verified software is loaded during the system boot process. This helps defend against malware and unauthorized software tampering. Implementing these measures significantly reduces cybersecurity risks and enhances the overall security posture of your system. By adhering to these guidelines, you can better protect your data, maintain the integrity of your system, and mitigate potential threats. 4.3 Environmental information Disposal Information Waste Electrical and Electronic Equipment (WEEE) This symbol on the product indicates that, under the European Directive 2012/19/EU governing waste from electrical and electronic equipment, this product must not be disposed of with other municipal waste. Please dispose of your waste equipment by handing it over to a designated collection point for the recycling of waste electrical and electronic equipment. To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate these items from other types of waste and recycle them responsibly to promote the sustainable reuse of material resources. For more information about recycling of this product, please contact your local city office or your municipal waste disposal service. For details, please visit the Barco website at: http://www.barco. com/AboutBarco/weee Turkey RoHS compliance Trkiye Cumhuriyeti: AEEE Ynetmeliine Uygundur.

[Republic of Turkey: In conformity with the WEEE Regulation]

23 Important information RoHS Chinese Mainland RoHS RoHS Barco/RoHSMCV According to the Management Methods for the Restriction of the Use of Hazardous Substances in Electrical and Electronic Products (Also called RoHS of Chinese Mainland), the table below lists the names and contents of toxic and/or hazardous substances that Barcos product may contain. The RoHS of Chinese Mainland is included in the MCV standard of the Ministry of Information Industry of China, in the section Limit Requirements of toxic substances in Electronic Information Products.

() Component name Hazardous substances and elements Printed Circuit Assemblies Pb X Hg O Cd O Cr6+

O PBB O PBDE O LCD panel

() External Cables Internal wiring Metal enclosure Plastic enclosure

() Heatsinks Battery Power Supply Unit Paper Manuals CD manual X X O O O O O X O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O O SJ/T 11364 This table is prepared in accordance with the provisions of SJ/T 11364. O: GB/T 26572 . O: Indicates that this toxic or hazardous substance contained in all of the homogeneous materials for this part is below the limit requirement in GB/T 26572. X: GB/T 26572 . X: Indicates that this toxic or hazardous substance contained in at least one of the homogeneous materials used for this part is above the limit requirement in GB/T 26572. EIP EFUPBarcoEFUP All Electronic Information Products (EIP) that are sold within Chinese Mainland must comply with the Marking for the restriction of the use of hazardous substances in electrical and electronic product of Chinese Mainland, marked with the Environmental Friendly Use Period (EFUP) logo. The number inside the EFUP logo that Barco uses (please refer to the photo) is based on the General guidelines of environment-friendly use period of electronic information products of Chinese Mainland. 24 Important information 10 RoHS/ China RoHS SDoC mark This product meets the requirements of the Management Rule on the Use Restriction of Hazardous Substances in Electrical and Electronic Products and the Management Catalogue for the Use Restriction of Hazardous Substances in Electrical and Electronic Products. SDoC The green SDoC mark is visible in the digital version of this document. 4.4 Biological hazard and returns Decommissioning Decommissioning When a device becomes obsolete or unusable, or is no longer needed by the health care facility, it enters the final stage of its life cycle: decommissioning. Decommissioning is the process of disposing a device, or removing a device from its originally intended use in the health care facility to an alternative use. Every health care facility or institution shall have standard operating procedures in place to decommission a device according to the Occupational Safety and Health Administration (OSHA) regulations or/and the World Health Organization (WHO) Decommissioning Medical Devices Technical guideline. The seller / manufacturer of the device has no legal obligation on the device sold in the event that the health care facility or institution decides to activate the decommissioning process. Overview The structure and the specifications of this device as well as the materials used for manufacturing makes it easy to wipe and clean and therefore suitable to be used for various applications in hospitals and other medical environments, where procedures for frequent cleaning are specified. However, normal use shall exclude biological contaminated environments, to prevent spreading of infections. Therefore use of this device in such environments is at the exclusive risk of Customer. In case this device is used where potential biological contamination cannot be excluded. Customer shall implement the decontamination process as defined in the latest edition of the ANSI/AAMI ST35 standard on each single failed Product that is returned for servicing, repair, reworking or failure investigation to Seller (or to the Authorized Service Provider). At least one adhesive yellow label shall be attached on the top site of the package of returned Product and accompanied by a declaration statement proving the Product has been successfully decontaminated. Returned Products that are not provided with such external decontamination label, and/or whenever such declaration is missing, can be rejected by Seller (or by the Authorized Service Provider) and shipped back at Customer expenses. 25 Important information 4.5 Regulatory information Intended Purpose MUIP-2213 is a general hardware platform for use in the hospital environment. It can be used for third party software applications that provide a user interface for medical systems. The equipment can be used in CathLab Examination Rooms & Control Rooms, Surgical Rooms and Hybrid Operating Rooms, both inside and outside the patient area. The equipment is not intended to be used for displaying medical images, nor for diagnostic purposes. Factory address Fimi S.r.l., Via Saul Banfi 1, 21047 Saronno, VA, Italy Manufacturing country The manufacturing country of the product is indicated on the product label (Made in ). Importers contact information To find your local importer, contact one of Barcos regional offices via the contact information provided on our website (www.barco.com). FEDERAL COMMUNICATIONS COMMISSION INTERFERENCE STATEMENT FCC class B 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. This device 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 device 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 device does cause harmful interference to radio or television reception, which can be determined by turning the device off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

Increase the separation between the device and receiver. Reorient or relocate the receiving antenna. Connect the device into an outlet on a circuit different from that to which the receiver is connected. Consult the dealer or an experienced radio/TV technician for help. Changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. RF Exposure Information (SAR) This device meets the governments requirements for exposure to radio waves. This device is designed and manufactured not to exceed the emission limits for exposure to radio frequency (RF) energy set by the Federal Communications Commission of the U.S. Government. The exposure standard employs a unit of measurement known as the Specific Absorption Rate, or SAR. The SAR limit set by the FCC is 1.6 W/kg. Tests for SAR are conducted using standard operating positions accepted by the FCC with the EUT transmitting at the specified power level in different channels. The FCC has granted an Equipment Authorization for this device with all reported SAR levels evaluated as in compliance with the FCC RF exposure guidelines. SAR information on this device is on file with the FCC and can be found under the Display Grant section of www.fcc.gov after searching on FCC ID: SXEAX210NGW. 26 Canada, Industry Canada (IC) Notices This device contains licence-exempt transmitter(s)/receiver(s) that comply with Innovation, Science and Economic Development Canadas licence-exempt RSS(s). Operation is subject to the following two conditions:

Important information

(1) This device may not cause interference.

(2) This device must accept any interference, including interference that may cause undesired operation of the device. Canada, avis d'Industry Canada (IC) Lmetteur/rcepteur exempt de licence contenu dans le prsent appareil est conforme aux CNR dInnovation, Sciences et Dveloppement conomique Canada applicables aux appareils radio exempts de licence. Lexploitation est autorise aux deux conditions suivantes :

1. Lappareil ne doit pas produire de brouillage;

2. Lappareil doit accepter tout brouillage radiolectrique subi, mme si le brouillage est susceptible den compromettre le fonctionnement. Radio Frequency (RF) Exposure Information The radiated output power of the Wireless Device is below the Industry Canada (IC) radio frequency exposure limits. The Wireless Device should be used in such a manner such that the potential for human contact during normal operation is minimized. This device has been evaluated for and shown compliant with the IC Specific Absorption Rate (SAR) limits when operated in portable exposure conditions. Informations concernant l'exposition aux frquences radio (RF) La puissance de sortie mise par lappareil de sans fil est infrieure la limite d'exposition aux frquences radio d'Industry Canada (IC). Utilisez lappareil de sans fil de faon minimiser les contacts humains lors du fonctionnement normal. Ce dispositif a t valu pour et dmontr conforme la Taux IC d'absorption spcifique ("SAR") des limites lorsqu'il est utilis dans des conditions d'exposition portatifs. FCC responsible: Barco Inc., 3059 Premiere Parkway Suite 400, 30097 Duluth GA, United States, Tel: +1 678 475 8000 Canadian notice CAN ICES-003 (B) / NMB-003(B) UKCA compliance Authorised representative in the UK: Barco UK Ltd, Building 329, Doncastle Road, Bracknell RG12 8PE, Berkshire, United Kingdom 27 Important information 4.6 EMC notice General information This device is suitable for use in professional healthcare facility environments only With the installation of the device, use only the delivered external cables and power supply or a spare part provided by the legal manufacturer. Using another can result in a decrease of the immunity level of the device. WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. WARNING: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation. WARNING: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the MUIP-

2213, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. Electromagnetic emissions The MUIP-2213 is suitable for use in the electromagnetic environment specified below. The customer or the user of the MUIP-2213 should assure that it is used in such an environment. Emissions test RF emissions CISPR 11 RF emissions CISPR 11 Harmonic emissions IEC 61000-3-2 Voltage fluctuations/ flicker emissions IEC 61000-3-3 Compliance Group 1 Class B Class D (1) Complies Electromagnetic environment Guidance The MUIP-2213 uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment. The MUIP-2213 is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-

voltage power supply network that supplies buildings used for domestic purposes. This MUIP-2213 complies with appropriate medical EMC standards on emissions to, and interference from surrounding equipment. 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. Interference can be determined by turning the equipment off and on. If this equipment does cause harmful interference to, or suffer from harmful interference of, surrounding equipment, the user is encouraged to try to correct the interference by one or more of the following measures:

Increase the separation between the equipment and receiver. Reorient or relocate the receiving antenna or equipment. Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. Consult the dealer or an experienced technician for help. Electromagnetic immunity The MUIP-2213 is tested to be used in the electromagnetic environment specified below. The customer or the user of the MUIP-2213 should assure that it is not used in an environment that exceeds the listed test levels and limits. 28 1. Active power for MUIP-2213 is less than 75 W 2. Immunity test IEC 60601 test levels Compliance level Electrostatic discharge

(ESD) IEC 61000-4-2 8 kV contact 2 kV, 4 kV, 8 kV, 15 kV air 8 kV contact 2 kV, 4 kV, 8 kV, 15 kV air Electrical fast transient/

burst IEC 61000-4-4 Surge IEC61000-4-5 Input AC/DC Power Ports:

2 kV 5 / 50 Tr/Th (ns) 100 Repetition frequency (kHz) I/O and Communication Port:

1 kV 5 / 50 Tr/Th (ns) 100 Repetition frequency (kHz Line to line: 0.5 kV, 1 kV Line to ground: 0.5 kV, 1 kV, 2 Kv. Input AC/DC Power Ports:

2 kV 5 / 50 Tr/Th (ns) 100 Repetition frequency (kHz) I/O and Communication Port:

1 kV 5 / 50 Tr/Th (ns) 100 Repetition frequency (kHz Line to line: 0.5 kV, 1 kV Line to ground: 0.5 kV, 1 kV, 2 kV Important information Electromagnetic environment guidance Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%

Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 0% residual voltage for 0.5 period at 0, 45, 90, 135, 180, 225, 270 and 315 0% residual voltage for 1 period at 0 70% residual voltage for 25 periods at 0 Voltage interruptions: 0%

residual voltage for 250 periods at 0 0% residual voltage for 0.5 period at 0, 45, 90, 135, 180, 225, 270 and 315 0% residual voltage for 1 period at 0 70% residual voltage for 25 periods at 0 Voltage interruptions: 0%

residual voltage for 250 periods at 0 Mains power quality should be that of a typical commercial or hospital environment. If the user of the MUIP-2213 requires continued operation during power mains interruptions, it is recommended that the MUIP-2213 be powered from a battery Power frequency magnetic field IEC 61000-4-8 Conducted RF IEC 61000-4-6 Radiated RF IEC 61000-4-3 50 or 60 Hz 30 A/m 50 or 60 Hz 30 A/m 3 Vrms (6 Vrms in ISM bands & amateur radio band) 150 kHz to 80 MHz 3 Vrms (6 Vrms in ISM bands & amateur radio band) 150 kHz to 80 MHz Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment If there is a mark on the device as shown on the right symbol, the device can be located near the interference may occur 3 V/m or 10 V/m

( depends on operating environment, home environment 10V; medical environment 80 MHz to 2.7 GHz 29 Important information Proximity magnetic fields IEC 61000-4-39 8 A/m 30 kHz CW 8 A/m 30 kHz CW 65 A/m 134.2 kHz 2.1 kHz Pulse modulation 65 A/m 134.2 kHz 2.1 kHz Pulse modulation 7.5 A/m 13.56 MHz 50 kHz Pulse modulation 7.5 A/m 13.56 MHz 50 kHz Pulse modulation Immunity to RF wireless communications equipment Test frequency

(MHz) Band (MHz) Service Modulation Maximum power (W) Distance

(m) Immunity test level (V/

m) 385 380 390 TETRA 400 450 430 470 GMRS 460, FRS 460 710 745 780 810 870 930 1720 1845 1970 704 787 LTE Band 13, 17 800 960 GSM 800/

900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5 1700 1990 GSM 1800, CDMA 1900, GSM 1900, DECT, LTE Band 1/3/4/

25, UMTS Pulse modulation 18 Hz FM 5 kHz deviation 1 kHz sine Pulse modulation 217 Hz Pulse modulation 18 Hz Pulse modulation 217 Hz 2450 2400 2570 5100 5800 5240 5500 5785 Bluetooth, WLAN, 802.11 b/g/n, RFID 2450, LTE Band 7 W LAN 802.11 a/n Pulse modulation 217 Hz Pulse modulation 217 Hz 1.8 2 0.3 0.3 0.2 0.3 27 28 9 2 2 2 0.3 28 0.3 28 0.3 28 0.2 0.3 9 30 4.7 Explanation of symbols Symbols on the device On the device or power supply, you may find the following symbols (nonrestrictive list):

Important information Indicates the device meets the requirements of the applicable EC directives/

regulations. Indicates compliance with Part 15 of the FCC rules (Class A or Class B) Indicates the device is approved according to the UL Recognition regulations Indicates the device is approved according to the UL Demko regulations Indicates the device is approved according to the CCC regulations 31 Important information Indicates the device is approved according to the VCCI regulations Indicates the device is approved according to the KC regulations Indicates the device is approved according to the BSMI regulations Indicates the device is approved according to the PSE regulations Indicates the device is approved according to the RCM regulations Indicates the device is approved according to the EAC regulations IS 13252 (Part 1) IEC 60950-1 Indicates the device is approved according to the BIS regulations R-xxxxxxxx www.bis.gov.in Indicates the device is approved according to the INMETRO regulations. Indicates the device is approved according to the UKCA regulations. Indicates the USB connectors on the device Indicates the DisplayPort connectors on the device 32 Indicates the entity importing the device into the locale. Important information Indicates 10 C to 35 C for units provided with battery pack to safely operate within specs. Indicates 10 C to 40 C for units provided without battery pack to safely operate within SN REF Indicates the device serial number Indicates the device part number or catalogue number Remove the square of SN & REF Warning: dangerous voltage Caution Please carefully read and follow the instructions and warnings on the label to ensure safe use. Consult the Instructions For Use Indicates this device must not be thrown in the trash but must be recycled, according to the European WEEE (Waste Electrical and Electronic Equipment) directive Indicates Direct Current (DC) Indicates Alternating Current (AC) Stand-by 33 Important information Symbols on the box On the box of the device, you may find the following symbols (nonrestrictive list):

Indicates a device that can be broken or damaged if not handled carefully when being stored. Indicates a device that needs to be protected from moisture when being stored. Indicates the storage direction of the box. The box must be transported, handled and stored in such a way that the arrows always point upwards. n 15 Indicates the maximum number of identical boxes which may be stacked on each other, where n is the limiting number. n or xx-yy Kg or yy xx-yy Indicates the weight of the box and that it should be carried with two persons. Indicates that the box should not be cut with a knife, a cutter or any other sharp object. Indicates the temperature limits4 to which the device can be safely exposed when being stored. Indicates the range4 of humidity to which the device can be safely exposed when being stored. Indicates the range4of atmospheric pressure to which the device can be safely exposed when being stored. 4.8 Legal disclaimer Disclaimer notice Although every attempt has been made to achieve technical accuracy in this document, we assume no responsibility for errors that may be found. Our goal is to provide you with the most accurate and usable documentation possible; if you discover errors, please let us know. 3. Values for xx and yy can be found in the technical specifications paragraph. 34 Important information Barco software products are the property of Barco. They are distributed under copyright by Barco NV or Barco Inc., for use only under the specific terms of a software license agreement between Barco NV or Barco Inc. and the licensee. No other use, duplication, or disclosure of a Barco software product, in any form, is authorized. The specifications of Barco products are subject to change without notice. Trademarks All trademarks and registered trademarks are property of their respective owners. Copyright notice This document is copyrighted. All rights are reserved. Neither this document, nor any part of it, may be reproduced or copied in any form or by any means - graphical, electronic, or mechanical including photocopying, taping or information storage and retrieval systems - without written permission of Barco. 2022 Barco NV all rights reserved. Product Security Incident Response As a global technology leader, Barco is committed to deliver secure solutions and services to our customers, while protecting Barcos intellectual property. When product security concerns are received, the product security incident response process will be triggered immediately. To address specific security concerns or to report security issues with Barco products, please inform us via contact details mentioned on https://www.barco.com/psirt. To protect our customers, Barco does not publicly disclose or confirm security vulnerabilities until Barco has conducted an analysis of the product and issued fixes and/or mitigations. 4.9 Technical specifications Overview Description Configuration for MUIP-2213 STxW wwww Processor (SoC) Intel Pentium N6415, Quad Core @1.2GHz, 1.5 MB L2 Cache. BIOS INSYDE Operating System Microsoft Windows 10 Iot LTSC / 11 Iot LTSC Networking Memory Built-in Gigabit Ethernet LAN interfaces (2 ports) 8 GB DDR4 3200MHz RAM (module) Local Storage 128 GB M.2, PCIE module Option Storage 256GB M.2, SATA module LCD Panel Characteristics 13.3 TFT LCD 1920 x 1080 pixels resolution. Audio System 1x (3in1) Audio Earphone Jack USB 2 x USB 3.0 type A port 5V/0.9A,4.5W,total 9.0W 1 x USB 3.2 type C port under the rear cable cover 5V/0.9A,4.5W Buttons and Controls Power button on bottom-right side Input device Touchscreen multi-touch (PCAP technology) Power source input 19VDC or 12-24V Internal battery for MUIP-

MUIP-2213 STxW wwww 4170 mAh / 7.2 Vdc (not removable) avoids UI crash in case of mains power drop 35 Important information Protection against electrical shocks Class II Power supply external AC-DC power supply Operating temperature (for safety) 10 C to 35 C for units provided with battery pack Operating temperature (for performance) 10 C to 35 C Operating humidity 20% to 80% for performance / 10% to 90% for safety (non-condensing) Storage temperature

-20 C to 50 C Storage humidity 10% to 90% (non-condensing) Storage altitude 70 to 110 kPa Operating altitude 3000 m (Max) Ingress protection IPX3,(IPx0 for the external power supply) Durability Weight Rugged anti-shock design 1.86 kg (typical) without desktop support 2.21 kg (typical) with desktop support Dimensions (W x H x D) 334 x 226 x 38 mm Certifications & compliance China: CCC Europe: CE (ITE), DEMKO US and Canada: UL, FCC, ICES-003 Japan: VCCI Australia: RCM AAMI ES60601-1:2005, ES60601-1:2005/AMD1 1:2012, ES60601-1:2005/

AMD2:2021 CAN/CSA-C22.2 NO. 60601- 1:14/A2:2022 IEC 60601-1:2005, AMD1:2012, AMD2:2020 EN 60601-1:2006/A1:2013/A12:2014/A2:2021 IEC 62368-1: 2018 EN IEC 62368-1:2020+A11:2020 IEC 60601-1-2: 2014 +A1:2020 EN 60601-1-2: 2015 +A1:2021 EMI specific:

FCC part 15 Class B ICES-003 Level B GB17625.1-2022, GB4943.1-2022, GB/T 9254.1-2021 Standards 36 Important information Overview Description Configuration for MUIP-2213 STxW wwww Processor (SoC) Intel Pentium N6415, Quad Core @1.2GHz, 1.5 MB L2 Cache. BIOS INSYDE Operating System Microsoft Windows 10 Iot LTSC / 11 Iot LTSC Networking Memory Local Storage Option Storage Built-in Gigabit Ethernet LAN interfaces (2 ports) 8 GB DDR4 3200MHz RAM (module) 128 GB M.2, PCIE module 256GB M.2, SATA module LCD Panel Characteristics 13.3 TFT LCD 1920 x 1080 pixels resolution. Audio System 1x (3in1) Audio Earphone Jack USB Buttons and Controls Input device Output 2 x USB 3.0 type A port 5V/0.9A,4.5W, total 9.0W 1 x USB 3.2 type C port under the rear cable cover 5V/0.9A,4.5W Power button on bottom-right side, reset pin-hole under connector cover Touchscreen multi-touch (PCAP technology) Support Type C dongle transfer HDMI out Power source input 19VDC or 12-24V Protection against electrical shocks Power supply Class II external AC-DC power supply Operating temperature (for safety) Operating temperature (for performance) 10 C to 40 C for units provided without battery pack 10 C to 35 C Operating humidity 20% to 80% for performance / 10% to 90% for safety (non-condensing) Storage temperature

-20 C to 50 C Storage humidity 10% to 90% (non-condensing) Storage altitude Operating altitude 70 to 110 kPa 3000 m (Max) Ingress protection IPX3,(IPx0 for the external power supply) Durability Weight Dimensions (W x H x D) Rugged anti-shock design 1.68 kg (typical) without desktop support 2.03 kg (typical) with desktop support 334 x 226 x 38 mm Certifications & compliance China: CCC Europe: CE (ITE), DEMKO US and Canada: UL, FCC, ICES-003 Japan: VCCI Australia: RCM 37 Important information Standards AAMI ES60601-1:2005, ES60601-1:2005/AMD1 1:2012, ES60601-

1:2005/

AMD2:2021 CAN/CSA-C22.2 NO. 60601- 1:14/A2:2022 IEC 60601-1:2005, AMD1:2012, AMD2:2020 EN 60601-1:2006/A1:2013/A12:2014/A2:2021 IEC 62368-1: 2018 EN IEC 62368-1:2020+A11:2020 IEC 60601-1-2: 2014 +A1:2020 EN 60601-1-2: 2015 +A1:2021 EMI specific:

FCC part 15 Class B ICES-003 Level B GB17625.1-2012; GB4943.1-2011; GB/T9254-2008 Identification label position The product identification label is located at the back of the MUIP-2213 as illustrated below. Image 41 Code number (12NC or K code) : (Model No.) Serial, number: 72yyww000000 72 = Original code (FIMI) yy = Year ww = Week (01 to 52) Manufacturer-Date 000000 = 6-digits progressive number 38 Important information K5902132 (451920612535) /04 | 2022-03-10 www.barco.com 39

WIFI + RFID FCC LABEL 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. CAN ICES-3 (BYNMB-3(8) Fe OoAZ

| Contains FCC ID: SXEAX210NGW | FCC ID: SXEMUIP2213RF Contains IC: 9393B-AX210NGW IC: 9393B-MUIP2213RF RFID ONLY FCC LABEL This device complies with part 15 of the FCC Rules. ation is subject to the following two conditions:

(1) this device may not cause harmful interference, and 35

(2) this device must accept any interference received including interference that may cause undesired operation. CAN ICES-3 (BYNMB-3(B) 10:

Fe OAZ FCC ID: SXEMUIP2213RF 9393B-MUIP2213RF BAe @OGAO cL us PIN (= 883) Model / Type {IF 22737 MUP ZTS STF nONT aGEZe2T FE: 0

(85/8855) CE YK fesse ag cA wy 2077 PROD OATE E 1422) 380 nian pach? | enzo ou ing(sk A) te2or 520 moe wuraty OQ 0 tate tay A ee

Barco N.V. President Kennedypark 35, Kortrjk 8500, Belgium Designation of U.S. Agent for Service of Process Certification Attestation Letter DATE: 27/07/2023 To: Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 USA ATTENTION: FCC Certification ~ Section 2.911(d)(7) Information Barco N.V. as required by section 2.911(d)(7), designate below contact located in the United States for purposes of acting as the applicant's agent for service of process. The Applicant acknowledges that they must maintain an agent for no less than one year after terminating all marketing and importation or the conclusion of any Commission-related proceeding involving the equipment. The applicant further acknowledges their responsibilty to inform the FCC whenever the Designated U.S. Agent information above changes. Applicant Signed: Designated U.S. Agent Signed:

sores, Cae Chie fied Printed name: Erie Chis Pred name: Roxana Alon Title: RD Manager Hardware Title: Global Quality & Compliance Officer Company Name: Barco 1. Company Name: Barco Ine Emel ec chu@berca com FRN: 0034043620 TEL +9256-299211 Emel roxna slen@barcocom Fax +32.56250211 TEL: +1 678475 000 Address: President Kemnedypark 35, Kok 8500, FAX:NA Belgium Address: 3059 Premiere Parkway Suite 400, 30097 Duluth GA

Certification Application Attestation Statements Barco N.V. President Kennedypark 35, Kortrijk 8500, Belgium To Whom It May Concern:

Statement for 47 CFR section 2.911(d)(5)(i) Barco N.V. certifies that as of the date of the application the equipment for which authorization is sought is not covered equipment1 prohibited from receiving an equipment authorization pursuant to section 2.903 of the FCC rules. If the equipment for which the applicant seeks authorization is produced by any of the entities identified on the current Covered List, including affiliates or subsidiaries of the named companies, the applicant must include an explanation on why the equipment is not covered equipment. Additional Explanation: <N/A>

Statement for 47 CFR section 2.911(d)(5)(ii) Barco N.V.certifies that, as of the date of the filing of this application, the applicant

- is /

- is not (3) identified on the Covered List as an entity producing covered equipment. Date:

City:

Name(2) :

Function:

Telephone number:

Email address:

Signature:

2023/07/27 Kortrijk Eric Chiu RD Manager Hardware

+32-56-233211 eric.chiu@barco.com 1 - The Commissions Covered List is published by the Public Safety and Homeland Security Bureau and posted on the Commissions website. This Covered List, which is periodically updated, identifies particular equipment, produced by particular entities, that constitutes covered equipment. https://www.fcc.gov/supplychain/coveredlist .

(2): For FCC it must be the Grantee Code owner or the authorized agent.

(3): double cllick on the appropriate box and select checked then OK Doc nr.

RF_160_05 Declaration of Authorisation Date of issue 02-01-2023 Declaration of Authorization We Name:

Address:

City:

Country:

Declare that:

Barco N.V. President Kennedypark 35, Kortrijk 8500, Belgium Kortrijk Belgium Name Representative of agent:

Agent Company name:

Address:

City:

Country Chenz Ker MRT Technology (Taiwan) Co., Ltd No. 38, Fuxing Second Rd., Guishan Dist., Taoyuan Taiwan is authorized to apply for Certification of the following product(s):

Product description: LCD USER INTERFACE FCC ID: SXEMUIP2213RF IC: 9393B-MUIP2213RF Type designation: MUIP-2213 Trademark:

BARCO on our behalf. Date:

City:

2023/07/27 Kortrijk Name:

Eric Chiu Function:

RD Manager Hardware Signature:

FCC, Request for non-disclosure RF_501, Issue 10 Date: 02-01-2022 Company Name: Barco N.V. Address:

City:

Country:

President Kennedypark 35, Kortrijk 8500, Belgium Kortrijk Belgium To: Kiwa Netherlands B.V., Dept. FCC TCB Wilmersdorf 50 7327 AC Apeldoorn The Netherlands Subject: Request for confidentiality FCC ID: SXEMUIP2213RF Reference number: ######

Dear FCC TCB, 1. Long-Term Confidentiality Pursuant to 47 CFR Section 0.459(a) & (b), we hereby requests non-disclosure and confidential treatment of the following materials submitted in support of FCC certification application:

Bill(s) of Material Block Diagrams Operational Description Schematic Diagrams Tune-up Procedure Above materials contain secrets, proprietary and technical information, which would customarily be guarded from competitors under 47 CFR, section 0.457(d)(2). Disclosure or publication or any portion of this company confidential material to other parties could cause substantial competitive harm and provide unjustified benefits for competitors. 2. Short-Term Confidentiality (STC) 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, applicant hereby requests Short-Term Confidential treatment of the following materials (See notes below):

Internal Photos Users Manual Test Set-up Photos External Photos Justification:

Name and signature of applicant: Eric Chiu Date: 2023/07/27 Notes:

1) A document or type of document can only have ONE type of confidentiality!

2) Short-Term confidentiality is in principle for 45 days from date of grant; it can be extended max 3 times (total time 180 days max.)!

The planned date should state in the RF731 application form. 3) FCC must be informed when marketing begins earlier. 4) Release takes place automatically thus extension must be requested in time. Telefication does not remind you of this!

5) Request for extension or for release must be received by Kiwa NL B.V. at least 7 days before date of actual marketing or before expiration of the STC period