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Recommended separation distances between

portable and mobile RF communications equipment and the

Sphygmomanometer (MD2000/MD2010/MD2040/MD2050/MD2001/MD2011/MD2041/MD2051/MD2090)

The 

Sphygmomanometer (MD2000/MD2010/MD2040/MD2050/MD2001/MD2011/MD2041/MD2051/MD2090)

 is 

intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The 
customer or the user of the 

Sphygmomanometer 

(MD2000/MD2010/MD2040/MD2050/MD2001/MD2011/MD2041/MD2051/MD2090) 

can help prevent 

electromagnetic interference by maintaining a minimum distance between portable and mobile RF 
communications equipment (transmitters) and the 

Sphygmomanometer 

(MD2000/MD2010/MD2040/MD2050/MD2001/MD2011/MD2041/MD2051/MD2090)

 

as recommended below, 

according to the maximum output power of the communications equipment. 

 

  

- 21 -

APPENDIX III

Содержание MD2000

Страница 1: ...LATION 7 USE THE OPTIONAL AC ADAPTER 8 SETTING DATE AND TIME 9 BEFORE TAKING A MEASUREMENT 10 APPLYING ARM CUFF 10 PERFORMING BLOOD PRESSURE MEASUREMENT 11 RECALL AVERAGE AND PREVIOUS MEASUREMENT DATA 12 DELETE MEASUREMENT DATA 12 PRESSURE BAR INDICATOR 13 WHO CLASSIFICATION INDICATOR 13 ABOUT IRREGULAR HEARTBEAT 14 ABOUT BLOOD PRESSURE 14 TROUBLESHOOTING 15 TECHNICAL SPECIFICATION 16 APPENDIX I 1...

Страница 2: ...be transmitted to pre approved mobile devices COMPLIANCE This device conforms to European Medical Device Directive 93 42 EEC This device complies with EN ISO 81060 standard relating to non invasive sphygmomanom eters Part 1 Requirements and test methods for non automated measurement types and EN 1060 standard relating to non invasive sphygmomanometers Part 3 Supplementary requirements for electro ...

Страница 3: ...place cardiac examination The WHO Blood Pressure Classification chart is a guide for reference and is not intended to replace medical diagnosis Use the device only as intended Do not use the device for any other purpose Do not apply the device on an arm with an unhealed wound or under medical treatment Do not take measurements more than necessary High measurement repetition rates may cause pain nu...

Страница 4: ...may shorten the life of the part Dispose used equipment parts batteries and optional accessories according to applicable local regulations Unlawful disposal may cause environmental pollution IMPORTANT NOTES If you have any of the following medical conditions you may get an inaccurate reading with the device Please consult your physician before using the device Patients in shock Cardiac arrhythmias...

Страница 5: ...hen storing the device make sure that no heavy objects are placed on top of it IMPORTANT NOTES Do not wrap the cuff around body parts other than your upper left arm Misuse represents a risk to your health Packaging materials are a deadly hazard for children and can cause suffocation Remove all packaging materials immediately and keep them away from children at all times Proper cuff size is importa...

Страница 6: ... 5 DEVICE DESCRIPTION Air Jack WHO LED Indicator Battery Cover DC Jack Memory Key Right Key Left Key Start Stop Key Display Main Unit Arm Cuff Air Plug Air Tube ...

Страница 7: ...ng Releasing Air Average Data Memory Record Number and Data Battery Indicator Pulse Rate Diastolic Pressure Systolic Pressure Irregular Heartbeat Indicator Heart Mark Severe Hypertension Moderate Hypertension Mild Hypertension High Normal Normal Optimal Pressure Bar User ...

Страница 8: ...ause a choking hazard to children Store the batteries out of the reach of children In case battery fluid leaks do not touch the battery fluid Avoid skin contact e g put on protective gloves and clean the battery compartment with dry cloth Remove the batteries from the battery compartment if the device will not be used for a long period Use only 1 5V alkaline batteries Do not use other types of bat...

Страница 9: ...ctrical outlet with wet hands When the AC adapter is in use the main unit does not draw power from batteries 8 USE THE OPTIONAL AC ADAPTER The AC Adapter 6VDC 600mA is an optional accessory and is sold separately A Connecting the AC adapter to the device 1 Insert the AC adapter output plug into the DC jack on the right side of the main unit 2 Plug the AC adapter into an AC outlet 3 The device will...

Страница 10: ...y to confirm and then HOUR will start to blink 8 Press or key to set the current Hour 9 Press key to confirm and then MINUTE will start to blink 10 Press or key to set the current Minute 11 Press key to confirm Date and time setting is completed 12 The device returns to Clock mode Date and time appear on the display B When device is in Clock Mode 1 Press or key to Standby Mode 2 Press and hold key...

Страница 11: ...ally tired or exhausted Remain still and do not talk during the measurement Position the cuff at heart level throughout the measurement Relax and sit comfortably on a chair Lay your feet flat on the floor Do not cross your feet Keep your back straight APPLYING ARM CUFF 1 Bare your left upper arm Make sure that the blood circulation in your arm in not constricted by any clothing that is too tight 2...

Страница 12: ...e monitor automatically determines your ideal inflation level and will stop inflation automatically When inflation completes deflation will start automatically The device is measuring the blood pressure and the pulse rate while the cuff is deflating Releasing air indicator the corresponding pressure bar indicators and the current cuff pressure appear on the display As soon as a pulse is detected t...

Страница 13: ...Clock Mode View average measurement data 1 In Clock Mode press or key to Standby Mode Press or key to select user number and press or to confirm 2 In Standby Mode press key to Memory Mode and view the average data of all previous measurement records in the memory 3 Press key to view AM average data of last 7 days AM measurement data 5 00 9 00 am 4 Press key to view PM average data of last 7 days P...

Страница 14: ... a snapshot of your blood pressure classification based on your measurements This will help you to understand what your blood pressure values mean Each segment of the bar indicator corresponds to the WHO blood pressure classification Pressurizing Releasing Air Inflation in progress Inflation complete Measurement in progress mmHg 110 105 100 95 90 85 80 Diastolic blood pressure 120 130 140 150 160 ...

Страница 15: ...inst the walls of the arteries Systolic pressure occurs when the heart contracts Diastolic pressure occurs when the heart expands Blood pressure is measured in millimeters of mercury mmHg One s natural blood pressure is represented by the fundamental pressure which is measured first thing in the morning while one is still at rest and before eating What Is Hypertension And How Is It Controlled Hype...

Страница 16: ...t ERROR code 3 E3 appears No pressure is detected The cuff may not fasten properly or too loose Reapply the cuff and fasten the cuff correctly ERROR code 5 E5 appears The cuff is over inflated Blood pressure over 300 mmHg It is recommended to consult your physician immediately ERROR code 6 E6 appears Low battery level Replace all used batteries with new batteries The monitor keeps re inflating Sys...

Страница 17: ...s MD2010 MD2050 MD2011 MD2051 MD2090 Dimensions Approx 4 6 x 6 1 x 3 117 x 154 x 75mm Cuff Size Arm Circumference Range Standard 9 13 22cm 32cm Large 13 17 32cm 44cm Full Range 9 17 22cm 44cm Operating Temperature 41 F to 104 F 5 C to 40 C Operating Humidity 15 to 93 RH Storage Temperature 13 F to 158 F 25 C to 70 C Storage Humidity up to 93 RH Operation storage and transport atmospheric pressure ...

Страница 18: ...t The Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 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 Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 is suitable for use in all establishments including domestic establi...

Страница 19: ... intended for use in the electromagnetic environment specified below The customer of the user of Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 should assure that it is used in such an environment Power frequency 50Hz 60Hz magnetic field IEC 61000 4 8 18 ...

Страница 20: ...40 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 should assure that it is used in such an environment Portable and mobile RF communications equipment should be used no closer to any part of the Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD201 1 MD2041 MD2051 MD2090 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmi...

Страница 21: ...ngth in the location in which the Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 is used exceeds the applicable RF compliance level above the Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or rel...

Страница 22: ...nment in which radiated RF disturbances are controlled The customer or the user of the Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2090 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the Sphygmomanometer MD2000 MD2010 MD2040 MD2050 MD2001 MD2011 MD2041 MD2051 MD2...

Страница 23: ... 22 ...

Страница 24: ...rning 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 technician for help WARNIN...

Страница 25: ...tability to five 5 years from the original date of purchase at retail This warranty extends only to the original retail purchaser and is not transferable G LAB s sole liability from this warranty is limited to replacement of defective product Under no circumstances shall G LAB be held liable for death or injuries to persons damage to property loss of use or any other special incidental contingent ...

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