DFMX User Manual Document Num:
User Manual JS02114DFMX V1.0 Version:
Issue Date:
Editor:
Reviewer:
Date:xx-xx-xx Date:xx-xx-xx History of Change:
Approver:
Date:xx-xx-xx Product Name: COMPER SMART DOPPLER FETAL MONITOR Product Model: DFMX Content Basic Function and Working Principle Overview Precautions, warnings and caution Explanation of Symbol Warnings and Cautions about Potential Electromagnetic Interference Warnings and cautions about chargeable lithium battery Product disposal The connection and remove of detachable components Usage schematic diagram of Fetal Monitor Charging tips Fetal monitoring knowledge Problems and Troubleshooting Cleaning and maintenance Storage and Shipping Condition Basic Parameters and Specifications The Registration Certificate Number and Production License Number Service Agencies and Information Table for acoustic output level Table for EMC Dear customers, Thank you for purchasing COMPER SMART DOPPLER FETAL MONITOR. Please read the user manual to ensure safe operation and accurate outcome before use. Keep this manual readily available for reference. Basic function of the product Fetal Monitor is hand-held detection instrument, intended to be used by health care professionals including obstetrician, nurse in hospitals, clinics and pregnant women at home. Application scope: monitor fetal heart sound and the range of heart rate during antepartum. Working principle Adopting the principle of non-focused ultrasound continuous wave Doppler, when the ultrasonic transducer generates an ultrasonic beam directing to the fetus. A portion of the incoming ultrasonic beam will reach the surface of fetal heart movement, due to the Doppler effect, the frequency shift of the ultrasonic occurs, which can be detected by receiving transducer. The low-frequency signal related to the fetal heart can be separated by signal processing, and to be identified. in use, Overview 1 2 3 4 Manual 5 Qualification certificate Parts list:
1. One Fetal Monitor 2. One pair of 3.5mm earphone 3. One USB charging cable 4. One manual 5. One qualification certificate 3 5 6 7 Power switch Volume down Volume up 4 1 2 Instruction of parts:
1. Charging socket 2. Earphone socket 3. Status indicator lamp 4. Power key 5. FH reading lamp 6. Volume keys 7. Doppler ultrasound probe Charging socket Earphone socket Precautions, warnings and caution All possible harms or damages caused by error operations have been indicated in this manual, please read these instructions. Please be aware and understanding that, for all human health and property damage due to error operations specified in the Manual or deviating from the designed purpose of the product, the Company shall not bear any responsibility. Prohibition It represents absolutely not allowed There may risk caused by operation that is out of the performance of the product. Warning Represent matters that require special attention May damage personal safety for the wrong purpose Caution Represent general considerations in using If misused, it may cause personal injury or property damage Explanation of Symbol Consult instruction for use Storage temperature limitation Serial Number Non-sterile Do not use if package is damaged Atmospheric pressure limitation Caution, consult accompanying document Type BF applied part non-ionizing radiation Warning!
The device is intended for detecting Fetal Heart Rate not intended for clinical treatment. If the result is distrustful, please use other methods to check the fetal well-being immediately. Environment conditions, operators and pregnant woman health conditions vary during device use, synthetic judgment are recommended in complex situation. Clean ultrasonic probe before use, it is high recommended for singe use to avoid cross - infection. Keep out reach of infants and young children. This product is ultrasonic product, and do not use it at the part other than the abdomen. Use the product matching earphone and charging cable. Using non-
matching accessories may lead to security risks of the product. Use the product supporting medical ultrasonic coupling agent, or similar products with a valid legal qualification of medical devices, otherwise it may cause the risk of biohazard or performance degradation. If the product breaks down during use, please shut down the power and turn to contact customer service for trouble shooting. Please inspect the bottom and surrounding of the ultrasonic probe before use and make sure there is no obvious damage which may affect the patient safety and instrument performance possibly. Caution!
Do not use the product close to strong electromagnetic fields, electromagnetic wave and magnetic environment
* There is possibility of measurement errors or damage to the product Avoid severe shock, falling from the height or stomping.
* There is possibility of causing damage to the product. On the premise of clinical requirement, it is recommended that users should minimize ultrasound exposure time. Do not place the product into boiling water for sterilization
* There is possibility of product breakdown or product failure. The product IP Rating is IPX4 (including ultrasound head) is a splashproof device, it can immerse in saline and water, but please do not soak in hot water. Except ultrasound head, other parts are designed of nonantisoak, please do not flush the product. Please wipe the product with a runout cloth to wipe the surface. Please do not wipe the product with disinfectant or alcohol or other organic solvent. Please wipe away the water with a dry cloth to keep maintenance. Please do not conduct ultrasonic cleaning, or it may cause a failure. Do not use a dryer, electric hair drier, otherwise it will cause a failure. 6 Warnings and Cautions about Potential Electromagnetic Interference Caution!
Warning!
In addition to the supporting earphone and charging cable, using unspecified accessories and cables may cause the increase of product radiation or the decline of immunity. This product should not be used closely to or stacked with other equipment, or if the close use or stacked use cannot be avoided, should observe and verify whether the product can operate normally in its configuration. Interference may occur in the vicinity of equipment marked with the symbol builtin rechargeable lithium battery, not removable, The device is please do not dismantle, damage the battery, heat the battery or throw it in fire. There is possibility of a battery explosion. Please shut down the product after use to avoid unnecessary Caution!
consumption of battery power. If the product is not to be used for more than 3 months, please store it in the environment of 10 C +40 C, otherwise there is a risk of damage to the battery. Warnings and cautions about chargeable lithium battery Product disposal Caution!
Please clean the remaining coupling agent after use, and wipe the product with cloth, twist dry come not to drip the dishcloth of water If the product becomes dirty, use a cloth or tissue paper with a small amount of water to wipe it clean. At the end of product life, please deal with the product according to the relevant local environmental protection laws and regulations. Caution!
Please conduct charging for at least 3 hours in the initial use of the Fetal Monitor. The product should be used with coupling agent. The product is equipped with the function of Bluetooth transmission 8 The connection and remove of detachable components Insert the plug of earphone into the earphone socket of Fetal Monitor;
In the process of charging, please insert the plug of USB charging cable into the charging socket of Fetal Monitor;
Make sure that the plug is fully inserted when connecting with the socket, and keep straight direction when removing. 9 Usage schematic diagram of fetal heart sound detector Starting up 1. Long press the power button, when the status indicator lamp shows white, indicating the starting up. 2. A liberal amount of coupling agent evenly spread onto abdomen. Prompt:
A thin layer of coupling agent is appropriate, in the process of searching fetal heart sound, if the coupling agent becomes drying or coagulating, it can be appropriately added. 10 Usage schematic diagram of fetal heart sound detector 3. The schematic diagram of listening to the fetal heart sound: please put on earphones, and then slowly move the Fetal Monitor to detect fetal heart rate, and the continuous regular heartbeat indicates the position of fetal heart, try to keep the unchanged position of Fetal Monitor (volume keys can be used to adjust the sound volume). 11 Usage schematic diagram of fetal heart sound detector 4. After a period of continuous monitoring of fetal heart sound, the different color of fetal heart sound reading lamp indicates the range of fetal heart rate, blue indicates the range of 120-160 beats/min, and orange indicates other ranges. Orange Blue
<120 beats/min
>160 beats/min 120~160 beats/min 5. After measurement, press the power button for 3 seconds, and extinction of light indicates power off. 3 seconds 12 6. Please wipe away the remaining coupling agent in abdomen and Fetal Monitor probe. 13 Charging tips Charging reminder When start up the product, the status indicator lamp blinks orange light, right after white light, alerting the low power, and please charge as soon as possible. If device wont turn on, please charge as soon as possible. After the charging is completed, the status indicator lamp shows blue light. status The charging cable is inserted into the charging socket, and the lamp shows orange light, which means the product enters into the state of charging. indicator 14 Fetal monitoring knowledge 1. In general, fetal heart sound can be monitored after 12 weeks of pregnancy, but because of individual differences, the gestational week that the fetal heart sound can be monitored may be different. 2. In general, the fetal heart rate is in the range of 120 to 160 beats / min, when the fetal heart rate is less than 120 beats /
min or more than 160 beats / min, consult with your physician depending on the individual situation. 3. When the pregnant woman finds that fetal heart sound cannot be found in the original location, but fetal movement can be felt, it indicates the fetal position may change. Slowly move the probe in small extent to find the fetal heart carefully. If you confirm that you cannot listen to the fetal heart sound or the fetal movement is not obvious, please go the hospital for consultation immediately. 15 Problems and Troubleshooting Problem/failure Cannot hear sound Noise is big Can hear the sound but it is relatively weak, and cannot find the fetal heart position Problem/failure The power switch turns on, but it is silent when rubbing the probe Noise is big Can hear the sound but it is relatively weak, and cannot find the fetal heart position Other failure Possible reason The volume is adjusted to the weakest Earphone is not inserted into the device No coupling agent is applied on the abdomen Noise is generated by the dragging of probe on the abdominal wall Incorrect placement of probe No coupling agent is applied on the abdomen Gestational age is short and fetal heart sound is too weak Possible reason Plug in your headphones and increase the volume Apply the coupling agent to the abdominal detection zone Find the fetal heart sound, lift up the probe and avoid dragging, and try to change the angle to get clear fetal heart sound Apply the coupling agent to the abdominal detection zone Use the product when the gestational stage is a little longer Please contact with Comper customer service Problems and Troubleshooting 16 Cleaning and maintenance Cleaning of Fetal Monitor the remaining coupling agent on Wipe away the ultrasonic probe. Be careful not to let the coupling agent, BB oil or other liquid get into the interior in order to avoid damage to the device. If there is a lot of dirt on the ultrasonic detector probe, please wipe the probe with a wringed cloth with neutral detergent or water, and then use a soft cloth to wipe it dry. Please disinfect the ultrasound probe, wipe gently with immersed medical cotton pad with 75% rubbing alcohol. Please comply with the following precautions to avoid breakdown or failure Do not remove dirt by using volatile agents, diluent or gasoline, etc. Do not immerse the product into in water or wash it with water. Do not use hot water to conduct sterilization (over 50 C). Turn off the power before cleaning; please keep it dry after cleaning Do not store the product in the following environments, or otherwise it will cause a breakdown or failure Humid environment High temperature, direct sunlight, dusty environment, or salt environment Environment with chemicals or corrosive gas 17 Storage and Shipping Condition Storage environment Temperature: -10C to +40C Humidity: 85% RH Ventilated room without corrosive gases Transportation environment Temperature: -40C to + 55C Humidity: 90% RH Atmospheric pressure: 50 to 101.3kPa Method: air, sea, rail transport or coach transport Basic Parameters and Specifications Battery: Rechargeable lithium battery (3.7V) Battery life: continuous use of 12 hours, more than 300 times of charge-
discharge Charging power supply: Micro USB (DC 5.0 V 160mA) The charging power supply should be checked or replaced regularly. Category of product Electric shock protection type: internal power supply Electric shock protection type: BF product Water proof level:
IPX4 (ultrasound probe) IPX1 (for the other part of housing) The degree of safety of combustible gas: not suitable for using in environment with flammable gas Operating mode: continuous operation Size of product: 46 x 39 x 135 mm Net weight: 150 g Communication: Ultra-low-power consumption Bluetooth 4.0 Standard Compliance AAMI/ANSIES606011:2005/(R)2012andA1:2012,,c1:2009/(r)2012anda2:2010/(r)2012
(consolidatedtext)medicalelectricalequipmentpart1:generalrequirementsforbasic safetyandessentialperformance(iec606011:2005,mod).(GeneralII(ES/EMC));
AAMI/ANSI/IEC6060112:2007/(R)2012,medicalelectricalequipmentpart12:general requirementsforbasicsafetyandessentialperformancecollateralstandard:
electromagneticcompatibilityrequirementsandtests(edition3).(GeneralII(ES/EMC));
IEC60601111IEC60601111Edition1.0201004,medicalelectricalequipmentpart1 11:generalrequirementsforbasicsafetyandessentialperformancecollateralstandard:
requirementsformedicalelectricalequipmentandmedicalelectricalsystemsusedinthe homehealthcareenvironment[including:technicalcorrigendum1(2011)].(GeneralII
(ES/EMC)) IEC606012372007MedicalelectricalequipmentPart237:Particularrequirementsfor thebasicsafetyandessentialperformanceofultrasonicmedicaldiagnosticandmonitoring equipment Basic Parameters and Specifications Working environment Temperature: + 15C to + 35C Humidity: 30%~90%
Atmospheric pressure: 70 to 106 kPa Product performance Rated sound working frequency: 2.0 MHz 10%
Ultrasonic output power: <10 mW Effective ultrasound emission area: <2.0 cm Comprehensive sensitivity: 90 dB Fetal heart monitoring range: 65 ~210 beats / min Fetal heart monitoring error: 2 times / min Continuous working time 2 hours
(Low battery or too large volume will shorten the working hours) Peak negative sound pressure: <0.2 MPa Sound intensity of output beam: 20 mW / cm Spatial peak time average output sound intensity:
<100 mW / cm Service life: 3 years 19 Service Agencies and Information Comper Chuangxiang
(Beijing)Technology Co.Ltd Building 1, Floor 3 Unit 712, 713, No. 3 Yongchang North Road, Economic and Technological Development Zone, Beijing US Agent Contact:
Name:
Contact number Manual version: JS02114DFMX V1.0 Table for acoustic output level COMPER How the best is done Copyright Copyright is owned by Comper (Beijing) Technology Co., Ltd., the Company shall enjoy and reserve all exclusive authority of copyright. No part of the Manual shall be increased or decreased, excerpted, reproduced, altered or imitated without the prior written consent of the Company. For the content of this Manual, the Company is not responsible for any explicit or implied warranty or guarantee liability. The content change caused by product improvements and technology updates could occur at any time without prior notice. The power of interpretation is vested by the Company. Federal Communications Commission (FCC) Statement 15.21 You are cautioned that changes or modifications not expressly approved by the part responsible for compliance could void the users authority to operate the equipment. 15.105(b) 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/TV technician for help. This device complies with part 15 of the FCC Rules. 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. This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. End users must follow the specific operating instructions for satisfying RF exposure compliance. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter. The procedures necessary for safe operation shall be provided, drawing attention to the safety hazards that may occur as a result of an inadequate electrical installation when the APPLIED PART of the ULTRASONIC DIAGNOSTIC EQUIPMENT is a TYPE B APPLIED PART. A notice shall be provided if the ULTRASONIC DIAGNOSTIC EQUIPMENT or parts thereof are provided with protective means against burns to the PATIENT when used with high frequency(HF) surgical equipment. If no such means are incorporated, notice shall be given in the ACCOMPANYING DOCUMENTS and advice shall be given regarding the location and use of the TRANSDUCER ASSEMBLY to reduce the hazard of burns in the event of defect in the HF surgical neutral electrode connection. A recommendation calling the OPERATOR'S attention to the need for regular testing and periodic maintenance including inspection of the TRANSDUCER ASSEMBLY for cracks that allow the ingress of conductive fluid shall be provided. Instructions shall be provided regarding the avoidance of unintended control settings and acoustic output levels. Guidance and manufacturers declaration-electromagnetic emissions The DFMX is intended for use in the electromagnetic environment specified below. The customer or the user of the DFMX should assure that it is used in such an environment. Emission test Compliance Electromagnetic environment-
guidance The DFMX 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 DFMX 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. RF emissions CISPR 11 Group 1 Class B Not applicable Not applicable RF emissions CISPR 11 Harmonic emissions IEC 61000-3-2 Voltage fluctuations
/flicker emissions IEC 61000-3-3 Guidanceandmanufacturersdeclarationelectromagneticimmunity The(DFMX)isintendedforuseintheelectromagneticenvironmentspecifiedbelow. Thecustomerortheuserofthe(DFMX)shouldassurethatitisusedinsuchanenvironment. Immunitytest Compliancelevel Electrostaticdischarge(ESD)IEC6100042 Electricalfasttransient/burstIEC6100044 SurgeIEC6100045 VoltageDips,shortinterruptionsandvoltagevariationson powersupplyinputlinesIEC61000411 IEC60601 testlevel
+6kVcontact
+8kVair
+2kVforpower supplylines
+1kVfor input/outputlines
+1kVline(s)to line(s)
+2kVline(s)to earth
<5%UT(>95%dip inUT)for0,5cycle 40%UT(60%dipin UT)for5cycles 70%UT(30%dipin
+6kVcontact
+8kVair Notapplicable Notapplicable Notapplicable Notapplicable Notapplicable Notapplicable Notapplicable Electromagneticenvironment guidance Floorsshould bewood, concreteorceramictile.If floorsarecoveredwith syntheticmaterial,therelative humidityshouldbeatleast 30%
Mainspowerqualityshouldbe thatofatypicalcommercialor hospitalenvironment. Mainspowerqualityshouldbe thatofatypicalcommercialor hospitalenvironment. Mainspowerqualityshouldbe thatofatypicalcommercialor hospitalenvironment.Ifthe userofthe(model) requirescontinuedoperation UT)for25cycles
<5%UT(>95%dip inUT)for5s Notapplicable Powerfrequency(50/60Hz)magneticfieldIEC6100048 3A/m 3A/m NOTEUTisthea.c.mainsvoltagepriortoapplicationofthetestlevel. duringpowermains interruptions,itis recommendedthatthe DFMXbepoweredfroman uninterruptiblepowersupply orabattery. TheDFMX powerfrequency magneticfieldsshouldbeat levelscharacteristicofatypical locationinatypicalcommercial orhospitalenvironment. The(DFMX)isintendedforuseintheelectromagneticenvironmentspecifiedbelow. Thecustomerortheuserofthe(DFMX)shouldassurethatisusedinsuchandenvironment. Immunitytest IEC60601testlevel Compliancelevel Guidanceandmanufacturersdeclarationelectromagneticimmunity ConductedRF IEC6100046 RadiatedRF IEC6100043 3Vrms 150KHzto80MHz 3V/m 80MHzto2,5GHz Notapplicable 3V/m Electromagneticenvironment guidance PortableandmobileRF communications equipmentshouldbeusedno closertoanypartofthe DFMXincludingcables,thanthe recommendedseparation distancecalculatedfromthe equationapplicabletothe frequencyofthetransmitter. Recommendedseparation distance:
d=1,2P d=1,2P80MHzto800MHz d=2,3P800MHzto2,5GHz WherePisthemaximumoutput powerratingofthetransmitterin watts(W)accordingtothe transmittermanufactureranddis therecommendedseparation distanceinmetres(m). FieldstrengthsfromfixedRF transmitters,asdeterminedbyan electromagneticsitesurvey,a shouldbelessthanthe compliancelevelineach frequencyrange.b Interferencemayoccurinthe vicinityofequipmentmarkedwith thefollowingsymbol:
NOTE1At80MHzand800MHz,thehigherfrequencyrangeapplies. NOTE2Theseguidelinesmaynotapplyinallsituations.Electromagneticpropagationisaffectedbyabsorptionandreflectionfromstructures,objectsand people. aFieldstrengthsfromfixedtransmitters,suchasbasestationsforradio(cellular/cordless)telephonesandlandmobileradios,amateurradio,AMandFM radiobroadcastandTVbroadcastcannotbepredictedtheoreticallywithaccuracy.ToassesstheelectromagneticenvironmentduetofixedRF transmitters,anelectromagneticsitesurveyshouldbeconsidered.IfthemeasuredfieldstrengthinthelocationinwhichtheDFMXisused exceedstheapplicableRFcompliancelevelabove,theDFMXshouldbeobservedtoverifynormaloperation.Ifabnormalperformanceis observed,additionalmeasuresmybenecessary,suchasreorientingorrelocatingtheDFMX. bOverthefrequencyrange150kHzto80MHz,fieldstrengthsshouldbelesthan3V/m. Recommendedseparationdistancebetween portableandmobileRFcommunicationsequipmentandtheDFMX TheDFMX isintendedforuseinanelectromagneticenvironmentinwhichradiatedRFdisturbancesarecontrolled.Thecustomerortheuserofthe DFMX canhelppreventelectromagneticinterferencebymaintainingaminimumdistancebetweenportableandmobileRFcommunicationsequipment
(transmitters)andtheDFMXasrecommendedbelow,accordingtothemaximumoutputpowerofthecommunicationsequipment. Ratedmaximumoutputpowerof Separationdistanceaccordingtofrequencyoftransmitter transmitter W 0,01 0,1 1 10 100 150kHzto80MHz d=1,2P N/A N/A N/A N/A N/A m 80MHzto800MHz d=1,2P 800MHzto2,5GHz d=2,3P 0,12 0,38 1,2 3,8 12 0,23 0,73 2,3 7,3 23 Fortransmittersratedatamaximumoutputpowernotlistedabove,therecommendedseparationdistancedinmeters(m)canbeestimatedusingthe equationapplicabletothefrequencyofthetransmitter,wherepisthemaximumoutputpowerratingofthetransmitterinwatts(W)accordingtothe transmittermanufacturer. NOTE1At80MHzand800MHz,theseparationdistanceforthehigherfrequencyrangeapplies. NOTE2Theseguidelinesmaynotapplyinallsituations.Electromagneticpropagationisaffectedbyabsorptionandreflectionfromstructures,objects andpeople.