User Manual
Contents
1.2. C a MONTH X DAY 3 5 Repeat step 2 and 3 to confirm YEAR BEFORE YOU START 6 After confirming the YEAR the LCD will display dOnE and the monitor will shut off rm T Ce Y Select User ID NOTE The monitor will shut off 60 seconds after the last operation when in User ID selection mode 4 When the monitor is OFF press and hold MEM button to enter User ID selection mode i 2 The current User ID ig blinks a 3 Press MEM button to switch between User 1 and User 2 A CIT 4 Press SET button to a confirm the selected User ID CI Lye BEFORE YOU START START MEASUREMENT v Pair up the Blood Pressure Monitor v Start Measurement with Your Device After correctly positioning the cuff and selecting User ID press START STOP 4 Tron Bluetooth and button to turn on the monitor and it will complete the measurement process the My BP Coach app Take User 1 for example Make sure both are ON proceeding l 16 E SYS mmis EF DIA mmg Pulmin 16 4 2 With the monitor OFF press and a mm2 manoaod ig 8 i 7 hold the START STOP button about i bo D DD 0 aaz LACER five seconds to start pair up until the symbol XR blinks indicating pair 3 Inflating and measuring 4 Display and save the result up igroceeding And the result will be transmitted to the app The icon X blinks 16 4 gt 1
3. C3 Bluetooth Contains FCC ID OU9AW8001 LS SMART Manufactured for Informed Clinical Sciences Corporation 1 Joy Street Boston MA USA 02108 www icsciences com GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO LTD Zone A 5 F Investment Building No 12 Huizhan East Rd Torch Development District Zhongshan Guangdong 528437 China Version 1 0 scile nces WWW ICSCIENCES COM User Manual IC Sciences Blood Pressure Arm Cuff Monitor TMB 1018 BT Arm Type D r A mmHg P Ulmin J Thank you for selecting the IC Sciences Blood Pressure Arm Cuff Monitor TMB 1018 BT Please read the user manual carefully and thoroughly to ensure safe usage of this product and keep the manual available for future reference Download and install My BP Coach from iTunes Store or Google play Esi 4 Download on the App Store TABLE OF CONTENTS Table of Contents INTRODUCTION tos triir ates sedate EENE Meco eewes ences teens EE e eet 2 e General Description e Indications For Use e Contraindications e Measurement Principle e Safety Information e LCD Display Signal e Monitor Components BEFORE VOW STARF epeteuvensteeeteeeobesat sates ea aA Ee E RE R E baw asaer 6 Power Supply Installing and Replacing the Batteries Apply the Cuff Settings Select User ID Pair up the Blood Pressure Monitor with Your Device START MEASUREMENT wi exiaied eared ei
4. ISO 10993 10 2010 It will not cause any potential alergic reaction or contact injury Please make sure the unit functions safely and it is in proper working conditions before use INTRODUCTION v LCD Display Signal eee LL LLO O OL B a 1 SYS mmHg E DIA mmHg x Pulimin om OOO O O0 188 INTRODUCTION v Monitor Components Component list of pressure measuring system fant Saws 1 Cuff T 0 a D 2 ree pipe K K K K T K METET CUFF 3 PCBA p e 4 Pump 5 Valve DESCRIPTION EXPLANATION Systolic Blood Pressure Top number Diastolic Blood Pressure Bottom number DC POWER SOCKET Pul min Pulse beat minute SET UP BUTTON START STOP BUTTON MEM DOWN BUTTON 4 User 1 Start measurement for user 1 save and transmit the measuring result automatically Q Start measurement for user 2 save and 2 User 2 transmit the measuring result automatically Memory Review Mode Indicate the current mode is memory review mode and which group of memory it is Successful Bluetooth Bluetooth is turned on Connection Average Value Average value of latest three records Error The monitor detects error List 1 Blood Pressure Monitor 2 Cuff Type BF Applied Part 22cm 42cm Low Batte Low battery replace the batteries 2 tae TMB 1018 BT Please use IC Sciences authorized cuff Unit Measurement unit of blood pressure Cu
5. b pressure Diastolic blood entering Systolic blood discharging artery pressure fluctuate throughout the day 1 Individual blood pressure varies throughout the day It can also be affected by the way you fasten your cuff and your measurement position take the measurement in the same position 2 Blood pressure varies even more when you on medication 3 Wait at least 3 minutes to take your blood pressure again What is the standard blood pressure classification The chart on the right illustrates the blood pressure classification mode by American Heart Association AHA This chart reflects blood pressure categories defined by American Heart Association Blood Pressure Category Systolic Diastolic mmHg upper mmHg lower Normal less than 120 less than 80 Prehypertension 120 139 Th AHA d High Blood Pressure 140 159 e AHA recommends e Secs v Why are measurements Followthesetips for the following guidelines P ae igh Blood Pressure 160 or higher 100 or higher z k for upper limit of normal Hypertension Stage 2 taken in the hospital correct to ensure correct blood pressure readings Pore e a ey Higher than 180 Higher than 110 readings at home different than those Make sure the cuffis fastened P correctly AHA Home Guideline for Upper Limit of Normal BP taken at home Make sure the the cuff is not too tight Blood pressure can be different Sree loose Systolic Bl
6. hold both MEM button and SET bution Keep the monitor at least 20 seats about 8 inches away ils pi human formeccend tociearmeion TELCO os eS ice Coie the head when the data transmission is proceeding after will display dEL dOnE indicating that the To enable the data transmission function this product should be paired to Bluetooth memory is cleared end at 2 4 GHz How to mitigate possible interference 1 The range between the device and BT end should be reasonably close from 1 meter to 10 meters about 3 to 30 feet Please ensure no obstacles are between the device and BT end to obtain a connection and to lower the RF output range 2 To avoid interference other electronic devices particularly those with wireless transmission Transmitter should be kept at least 1 meter about 3 feet away from the monitor 12 13 INFORMATION FOR USER INFORMATION FOR USER v Maintenance To obtain the best performance please follow the tips below v Tips for Measurement Your readings may be innaccurate if the measurement is taken in the following circumstances Avoid immersing in water Use and store in a dry place and Clean with a dry cloth avoid the sunshine xX Immediately measuring after tea coffee smoking Avoid shaking and dropping Avoid dusty environment and unstable temperatures Within 20 minutes x SSC after taking a bath Y Use a slightly damp cloth to remove the dirt Avoid washing
7. more information about our products and assistance please contact www icsciences com for customer service Manufactured for IC Sciences Company Informed Clinical Sciences Corporation Address 1 Joy Street Boston MA USA 02108 v Complied Standards List Risk Management ISO 14971 2007 Labeling EN 980 2008 Generl Requirements l l for Safety IEC 60601 1 2005 A1 2012 Performance and ANSI AAMI IEC 80601 2 30 2009 Clinical ANSI AAMI ISO 81060 2 2009 Requirements Electromagnetic Compatibility IEC 60601 1 2 2007 Software life cycle IEC 62304 2006 processes EMC GUIDANCE Caution The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance could void the user s authority to operate the equipment Note POTENTIAL FOR RADIO TELEVISION INTERFERENCE for U S A only This product has been tested and found to comply with the limits for a Class B digital device pursuant to Part 15 of FCC Rules These limits are designed to provide reasonable protection against harmful interference in a residential installation The product 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 the product does cause harmful interference to radio or television reception wh
8. pulsatile which is used to determine the systolic and diastolic pressure and pulse rate The device also compares the longest and the shortest time intervals of detected pulse waves to mean time interval then calculates standard deviation The device will display a warning signal with the reading to indicate the detection of irregular heartbeat when the difference of the time intervals over 2 INTRODUCTION v Safety Information The symbols below might be in the user manual on labeling or other components Symbol for THE OPERATION Symbol for TYPE BF APPLIED GUIDE MUST BE READ PARTS Symbol for ENVIRONMENT PROTECTION Waste electrical products should not be disposed of with household waste Please follow local guidelines Symbol for MANUFACTURE X DATE Symbol for MANUFACTURER symbol for DIRECT CURRENT u cey Symbol for Including RF S N Symbol for SERIAL NUMBER C tanemitier Bluetooth The Bluetooth Combination Mark CAUTION Please read this user manual carefully and thoroughly before use This device is intended for adult use in the home domestic only This device is intended for non invasive measuring and monitoring of arterial blood pressure It is not intended for use on extremities other than the upper arm or for functions other than obtaining a blood pressure measurement Do not confuse self monitoring with self diagnosis This unit
9. the cuff CAUTION 1 Make sure the unit functions safely and is in proper working order before use Don t service or maintain while the device is in use 2 If you have any problems with this device such as setting up maintaining or using please contact IC Sciences Do not open or repair the device yourself Ina very cold snvironment gt When you need to urinate 3 Please contact IC Sciences if any unexpected operation or events occur 4 Cleaning Dusty environments may affect the performance of the unit Please use a soft cloth to remove dirt from the device and cuff before and after use 5 Calibration The manufacturer does not require such preventive inspections or calibration by other persons and will make available on request of circuit diagrams component part list etc 6 Disposal Degraded sensors may result in inaccurate measurement while loosened electrodes may cause the monitor s failure to power on Please dispose of ACCESSORIES detachable 14 parts and ME EQUIPMENT according to local guidelines 15 ABOUT BLOOD PRESSURE ABOUT BLOOD PRESSURE What are systolic and diastolic pressures v Why does my blood When ventricles contract and pump blood out of the heart the blood pressure reaches its maximum value in the cycle which is called Wei systolic pressure When the ventricles relax the blood pressure reaches its minimum value in the cycle which is called diastolic PO relax 2 b 2
10. 2 SYS mmHg DIA mmng Pulimin If successful symbols rl a etal L i will be shown on the oe 18 88 tt OP Yau io oe LCD like the picture on ee a the right 42 SYS mmiis DIA mmis Pulini se CdJ o If devices fail to connect 3 008 0 a Da secs symbols will be shown on the LCD like the picture on the right If the data is successfully If the data transmission fails the MANEIRE MELEN LCD will display ERROR instead display dOnE 3 The monitor will shut off after pair up process is l complete 1e 8 Bluetooth Module No AW2540MV1 RF Frequency Range 2402 MHz to 2480 MHz Output Power Range 1 dBm 5 Press START STOP button to turn off the monitor Otherwise the monitor will shut off within 1 minute after last operation Supply Voltage 2 3 6 V Transmitting Distance 10 meters 32 feet Tips A Maximum 60 records are both for user 1 and user 2 10 11 DATA MANAGEMENT DATA MANAGEMENT v Recall the Records v Transmitting Data Manual Data Transmission 1 When the monitor is OFF press MEM 104 SYS mmus DIA meno Puli With the advanced Bluetooth 4 0 technology applied the mobile or portable button to retrieve the memory The monitor I E C 4 1C equipments which are equipped with Bluetooth function in line with BLE will display the average value of latest three t00 0 0 0 mA Technical Specific
11. allows you to monitor your blood pressure Do not start or end medical treatment without a physician s consent If you are taking medication consult your physician to determine the most appropriate time for your measurement Never change a prescribed medication without your physician s consent This unit is not suitable for continuous monitoring during medical emergencies or operations If the pressure of the cuff exceeds 40 kPa 300 mmHg the unit will automatically deflate Should the cuff not deflate when its pressure exceeds 40 kPa 300 mmHg detach the cuff from the upper arm and press the homologous button to stop inflation Do not use the monitor under the conditions of strong electromagnetic field e g mobile that radiates interference signal or electrical fast transient burst signal especially when the AC adaptor is applied Do not touch the output of batteries and the patient simultaneously The device is not AP APG equipment It is not suitable for use in the presence of a flammable anesthetic mixture with air or oxygen nitrous oxide Please keep the unit out of reach of infants or children since inhalation or swallowing of small parts is dangerous or even fatal Please use ACCESSORIES and detachable parts specified authorised by IC Sciences Otherwise it may cause damage to the unit or danger to the user patient The materials of the cuff have been tested and found to comply with requirements of ISO 10993 5 2009 and
12. ations as well as BLP Protocol established by global measurements y a organization Bluetooth SIG are capable to receive your personal health data gt When both the My BP Coach app and Bluetooth are ON TMB 1018 BT s will automatically transmit measurement data to your smartphone via Bluetooth 2 Press MEM button and SET button to rotate a the records Up to 60 records will be stored 42 SYS nmns DIA wry Putin I After measurement the symbol lights 42 SYS nmi DIA mens Pulm uhdercachuser iD ot 5 up indicating the measuring result is being etl Litt The measurement date and time will be om UL We a automatically transmitted to smartphone tit O98 Im iso displayed alternatively Cat D 12 3 2 f successful the LCD will display 3 If you would like to check another user i dOnE dG fe ID s history please follow the instructions in Select User ID to r a 8 change to another User ID first pad 3 If the devices fail to connect the LCD will display ERROR No Record found for User 2 CAUTION Interference may occur in the vicinity of equipment marked with the following symbol 2 And TMB 1018 BT may interfere other electrical equipment in the area v Delete the Records ict Sensitive people including pregnant women and those with implanted medical elec l a i i tronic devices should avoid using the unit whenever possible 1 When under data enquiry mode press E l E ai Ae and
13. bata w ocd op ed ae weed ee ieee aed oe bk 11 e Start Measurement DATA MANAGEMENT keii contents resets kaa E enna O E eee on eeet awe 12 e Recall the Records e Delete the Records e Transmitting Data INFORMATION FOR USER nec cetest stuertuesteetceee disuse ctu srin iE rieska ee 14 e Tips for Measurement e Maintenance ABOUT BLOOD PRESSURE a rcireripiperi sinuri dn eE bes Genes EEE 16 e What are systolic pressure and diastolic pressure e What is the standard blood pressure classification e Why does my blood pressure fluctuate throughout the day e Why are measurements taken in hospital different from at home e Is the result the same when measuring on the right arm TROUBLESHOOTING wetetneeteteoentadeosteteeents seceeet oes beets eeeesneee 18 SPECIFICATIONS wat eereeheeebutes eet aeyeus Gs cea ene uke coun cece ss ae ce 19 AUTHORIZED COMPONENT erien toredeke ed arenes a a ae omer 20 COMPLIED STANDARDS LIST sixvnaddeuepentnactdteadueatenedenaseceua 20 FCG SIAIEMENT ged derecadeeendueu hs cote cessed EEE ENEE EE AEE EEE 21 EMG GUDIANGCE p saaiii ieie saai Eni cutee tee aa araa E AE a ay 21 INTRODUCTION v General Description Thank you for selecting the IC Sciences Blood Pressure Arm Monitor TMB 1018 BT The monitor features blood pressure measurement pulse rate measurement and the data storage The design provides you with two years of storage Readings taken by the TMB 1018 BT are equivalent to those ob
14. ere 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 metres m Field strengths from fixed RF transmitters as deter mined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol o NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 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 the device is used exceeds the applicable RF compliance level above the device should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the device b Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m 23 Table 6 Recommended separation dis
15. ich can be determined by turning the product on off 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 product and the receiver Connect the product into an outlet on a circuit which is different from what the receiver is connected to Consult the dealer or an experienced radio TV technician for help v FCC Statement v EMC guidance Table 1 Guidance and MANUFACTURER S declaration ELECTROMAGNETIC EMISSIONS for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacturer s declaration electromagnetic emissions The device is intended for use in the electromagnetic environment specified below The customer or the user of the device should assure that it is used in such an environment Emissions test Compliance Electromagnetic environment guidance The device must emit electromagnetic Group 2 energy in order to perform its intended CISPR 11 4 function Nearby electronic equipment may be affected RF emissions RF emissions CISPR 11 Class B Harmonic emissions IEC 61000 3 2 Not applicable Voltage fluctuations flicker emissions Not applicable IEC 61000 3 3 22 Table 2 Guidance and MANUFACTURER S declaration electromagnetic IMMUNITY for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacturer s declaration electromagnetic immunit
16. ood Pressure 135 mm Hg Diastolic Blood Pressure 85 mm Hg v Irregular Heartbeat Detector This Blood Pressure Monitor is equipped with an intelligent function of Irregular Heartbeat IHB Detector During each measurement the arm cuff records the heartbeat intervals and determines the standard deviation If the calculated value is v s the result the same even during a 24 hour period because of the weather emotion exercise etc Especially white coat syndrome which makes results beginning higher than the ones at home Relax for 4 5 minutes before taking your blood pressure Take several deep breaths before larger than or equal to 15 this monitor will show the IHB symbol on the screen when displaying the measuring result CAUTION The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heartbeat was detected during measurement Usually this is NOT a cause for concern However if the symbol appears often we recommend you when measuring on the right arm It is ok to take readings in both arms but there may be different results for each arm Try to use the same arm every time seek medical advice Please note that the device does not replace a cardiac examination but serves to detect pulse irregularities at an early stage 16 17 TROUBLESHOOTING PROBLEM SYMPTOM CHECK THIS REMEDY Low batteries Error massage Batteries are exhausted Replace with ne
17. pital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the device requires continued operation during power mains interruptions it is recommended that the device be powered from an uninterruptible 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 NOTE Uzis the a c mains voltage prior to application of the test level Table 4 Guidance and MANUFACTURER S declaration electromagnetic IMMUNITY for ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Guidance and manufacturer s declaration electromagnetic immunity The device is intended for use in the electromagnetic environment specified below The customer or the user of the device should assure that it is used in such an environment IMMUNITY test Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 IEC 60601 TEST LEVEL 3 Vrms 150 kHz to 80 MHz 3 V m 80 MHz to 2 5 GHz Electromagnetic environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 167 JP d 1 167 4P 80 MHz to 800 MHz d 2 333VP 800 MHz to 2 5 GHz wh
18. portation condition Measurement perimeter of the upper arm Weight External dimensions Attachment Mode of operation Degree of protection Device Classification IP Classification Software Version SPECIFICATIONS Battery Powered Mode 6V 4 x AAA size batteries AC Adaptor Powered Mode 6V 1A Can be supplied by AC adaptor model UE08WCP 060100SPA Included Blue LCD with White Backlight V A 140mm L x 36mm W Oscillographic testing mode Pressure 0 40kpa 0 300mmHg pulse value 40 199 times minute Pressure 5 C 40 C within 0 4kpa 83mmHg pulse value 5 Temperature 5 C to 40 C 41 F to 104 F Relative humidity lt 85 Atmospheric pressure 86kPa to 106kPa Temperature 20 C to 60 C 4 F to 140 F RH 10 to 93 Atmospheric pressure 50kPa to 106kPa About 22cm 42cm 8 6 inches to 16 5 inches Approx 465g about 1 Ib Excluding batteries Approx 180 100 40mm approx 7 x 4 x 1 6 in 4 AAA batteries user manual Continuous operation Type BF applied part Battery Powered Mode Internally Powered ME Equipment AC Adaptor Powered Mode Class II ME Equipment IP22 V01 WARNING No modification of this equipment is allowed 19 AUTHORIZED COMPONENT v Authorized Component 1 Please use the included IC Sciences authorized adaptor Adaptor Type UEO8WCP 060100SPA Input 100 240V 50 60Hz 400mA Output 6V 1A Conforms to UL Certification v Contact Information For
19. rrent Time Month Day Hour Minute Irregular Heartbeat Detector 3 4xAAA batteries 4 User manual Detects irregular heart beats BEFORE YOU START BEFORE YOU START v Power Supply v Download and install My BP Coach 1 Battery powered mode s BVOC ASAAN batere from iTunes App store or Google play 2 AC adapt d mode A or powered mode v Apply the Cuff Can be supplied by AC adaptor model UE08WCP 060100SPA Included 1 Insert the plug of cuffs air pipe into the interface located on the right side of the monitor A E N adaptor Included Please unplug the adaptor to use battery power CAUTION g 2 As pictured on the right position In order to get the best effect and protect your monitor please use the the cuff on your upper arm battery and power adaptor which complies with U S safety standard 3 Tighten the cuff Make sure the cuff is fixed 2 to 3 centimeters about an inch above your elbow 1 Open the battery door 2 Insert the batteries according to the polarity indications j 3 Close the battery door You should be able to insert one finger when the cuff is tightened around your upper arm Replace the batteries under following circumstances bo Jaisplays on the Loo T to ISplays on the 4 Correct Posture The LCD display dims It is best to position the cuff on your bare e When powering on the monitor the LCD doesn t light up arm Sit comfor
20. tably and relaxed in a chair The center of the cuff should be about CAUTION e Remove batteries if the device is not likely to be used for some time even with your heart e Worn batteries are harmful to the environment Do not dispose with daily garbage Sit with legs relaxed with your feet falling outwards Rest your arm on a table with your palm facing up e Remove the old batteries from the device following your local recycling guidelines e Do not dispose of batteries in fire Batteries may explode or leak BEFORE YOU START Settings Set the time on your arm cuff before your initial use to ensure each record is labeled with a time stamp The range of the year is 2000 to 2050 Time Format 12 Hours NOTE The monitor will shut off 60 seconds after the last operation when in Setting Interface 4 When the monitor is OFF press and hold SET button to enter HOUR and MINUTE setting x 2 Press MEM button to See change the numeral Each ou it press will increase the numeral by one ina Cy CD cycling manner HOUR 3 Press SET button to confirm the HOUR and MINUTE Then the 60 co a e e gt D SS SS eee gt Y 2 X monitor diverts to s MONTH and DAY o setting MINUTE 4 Repeat step 2 and 3 to confirm MONTH and DAY Then the monitor switches to YEAR setting A a lt gt 10 ts ren D Ga Sd b
21. tained by a trained observer using the cuff and stethoscope auscultation method This manual contains important safety and care information and provides step by step instruction for using the product Read the manual thoroughly before using the product Features e Blue LCD display with white backlight e Up to 60 pieces of recorded data stored for each user e Measuring While Inflating MWI technology e Bluetooth data transmitting function v Indications For Use 1 The IC Sciences Blood Pressure Arm Monitor is a digital monitor intended for measuring blood pressure and heartbeat rate for people with an arm circumference ranging from 22cm to 42 cm about 8 66 16 5 inches 2 The monitor detects irregular heartbeats during measurement and gives a warning signal with readings 3 It is intended for adult use in the home setting only v Contraindications 1 The device is contraindicated for any person connected to a wearable or implantable electronic device or instrument such as a pacemaker or defibrillator 2 The device is not intended to be a diagnostic device Contact your physician if hypertensive values are indicated v Measurement Principle This product uses the Oscillometric Measuring method to detect blood pressure Before every measurement the unit establishes a zero pressure equivalent to the air pressure Then it starts inflating the arm cuff meanwhile the unit detects pressure oscillations generated by beat to beat
22. tances between portable and mobile RF communications equipment and the ME EQUIPMENT or ME SYSTEM for ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the device The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the device as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m Rated maximum output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 167 JP d 1 167 VP d 2333 P For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres 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 NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 24 29
23. w batteries Display will not Batteries are inserted Insert the batteries incorrectly correctly AC adaptor is inserted Insert the AC adaptor incorrectly tightly Display is dim or display m g Batteries are low Replace with new batteries 4 a Check if the APP is on or Data communication not try data transmission shows has failed again Inflation is slow or the Refasten the cuff and then cuff is not secure A Readjust the cuff not too loose or too tight and then measure again The pressure of the Refasten the cuff and then cuff is excess measure again light up Error 1 shows Error 2 shows The cuff is very tight Error 3 shows Retake the measurement If the problem persists contact the retailer or our customer service department for further assistance Refer to the warranty for contact information and return instructions Error 5 or Error 6 shows System error occurred The monitor detected Error 10 or Error 11 shows Relax for a moment and then motion talking or the measure again pluse is too poor while measuring The measurement Loosen clothing on the process does not detect arm and then measure the pulse signal again Error 21shows on The treatment of the Relax for a moment and the display measurement failed then measure again Error 20 shows Power supply Display mode Measurement mode Measurement range Accuracy Working condition Storage amp trans
24. y The device is intended for use in the electromagnetic environment specified below The customer or the user of the device should assure that it is used in such an environment IEC 60601 IMMUNITY test test level Electrostatic discharge ESD IEC 61000 4 2 6 kV contact 8 kV air Electrical fast transient burst IEC 61000 4 4 2 kV for power supply lines 1 kV for input output lines Surge 1 kV line s to line s IEC 61000 4 5 2 kV line s to earth Voltage dips short lt 5 Ur interruptions and gt 95 dip in Ur voltage variations for 0 5 cycle on power suppl ee 40 Ur input lines en 60 dip in Ur IEC 61000 4 11 for 5 cycles 70 Ur 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for5s Power frequency 50 60 Hz magnetic field IEC 61000 4 8 Compliance level 6 kV contact 8 kV air 2 kV for power supply lines 1 kV line s to line s lt 5 Ut gt 95 dip in Ur for 0 5 cycle 40 Ur 60 dip in Ur for 5 cycles 70 Ur 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for5s 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 hos
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