Model: MD6000 BM 81 easyLock EN Upper arm blood pressure monitor Instructions for use 18
ENGLISH Read these instructions for use carefully and keep them for later use, be sure to make them accessible to other users and observe the information they contain. Dear customer, Thank you for choosing a product from our range. Our name stands for high-quality, thoroughly tested prod ucts for applications in the areas of heat, weight, blood pressure, body temperature, pulse, gentle therapy, massage, beauty, air and baby. With kind regards Your Beurer team Contents 1. Included in delivery ...............
Product information Note on important information Observe the instructions Read the instructions before starting work and/or operating devices or machines Isolation of applied parts, type BF Galvanically isolated application part (F stands for “floating”); meets the requirements for leakage currents for type BF Direct current The device is suitable for use with direct current only Disposal Disposal in accordance with EC Directive WEEE (Waste Electrical and Electronic Equipment) Battery disposal Do not dispo
CE labelling This product satisfies the requirements of the applicable European and national directives 3. Intended use Intended use The blood pressure monitor is intended for the fully automatic, non-invasive measurement of arterial blood pressure and pulse values on the upper arm.
• Do not use the device at the same time as other medical electrical devices (ME equipment). This could lead to a malfunction of the device and/or an inaccurate measurement. • Do not use the device outside of the specified storage and operating conditions. This could lead to incorrect measurements. • O • P • Do not perform measurements more frequently than necessary. Due to the restriction of blood flow, some bruising may occur.
Notes on electromagnetic compatibility • The device is suitable for use in all environments listed in these instructions for use, including domestic environments. • The use of the device may be limited in the presence of electromagnetic disturbances. This could result in issues such as error messages or the failure of the display/device. • A void using this device directly next to other devices or stacked on top of other devices, as this could lead to faulty operation.
6. Initial use Inserting the batteries • R emove the battery compartment lid on the rear of the device. • Insert four 1.5 V AAA (alkaline type LR03) batteries. Make sure that the batter ies are inserted the correct way round. • C lose the battery compartment lid again carefully. • All display elements are briefly displayed, flashes in the display. Set the date and time as described below.
Date If the hour format is set as 12h, the day/month display sequence is reversed. Time The hour flashes on the display . • Using the +/- setting buttons, select your desired number for the hour and confirm with the M memory button. The minute flashes on the display . Bluetooth ® settings • Using the +/- setting buttons, select your desired number for the minute and confirm with the M memory button. The Bluetooth ® symbol flashes on the display.
• T with your upper arm circumference. The fit should be checked before measurement using the index mark described below. Ref. no. 164.290* Designation easyLock- Universal cuff Arm c ircumference 24-40 cm * Included in standard delivery • P must not be hindered by tight clothing or similar. The circulation of the arm • The device must be placed on the upper arm so that the bottom edge is positioned approx. 2–3 cm above the elbow. Adjust the device so that the “ARTERY ” mark is directly over the artery.
Adopting the correct posture • To carry out a blood pressure measurement, make sure you are sitting upright and comfortably. Lean back and place your arm on a surface. Do not cross your legs. Place your feet next to each other flat on the floor. • A • To avoid distorting the measurement, you should remain as still as possible during the measurement and not speak.
Measurement • If the Bluetooth ® function has been activated, the data transfer to the “beurer HealthManager” app starts automatically after the measurement. • The Bluetooth ® symbol flashes on the display. The device now attempts to connect to the app for approx. 30 seconds. • The Bluetooth ® symbol stops flashing as soon as the connection is established. All measurement data is transferred to the apps. Once the data transfer is successfully complete, the device switches off automatically.
Step 3: Take a measurement. Step 4: (Data transfer immediately following the measu rement): If the Bluetooth ® function has been activa ted, the data transfer to the „beurer HealthManager Pro“ or the „beurer HealthManager“ app starts automatically after the measurement. Step 4: (Data transfer at a later point in time): Go into the memory recall mode for the desired user me mory (see “Saving, accessing and deleting measu red values”). The data transfer starts automatically.
LED risk indicator The World Health Organization (WHO) has defined the internationally recognised classification for the evaluation of measured blood pressure values listed in the table below: Measured blood pressure value range Systole (in mmHg) Diastole (in mmHg) ≥ 180 160 – 179 140 – 159 130 – 139 120 – 129 < 120 ≥ 110 100 – 109 90 – 99 85 – 89 80 – 84 < 80 Classification Colour of the risk indicator High blood pressure stage 3 (severe) High blood pressure stage 2 (moderate) High blood pressure sta
Average values Individual measured values Deleting measured values PMflashes on the display. The average value of the evening measurements for the last 7 days is displayed (evening: 6.00 p.m. – 08.00 p.m.). • When you press the memory button M again, the last individual measurement is displayed (in this example, measurement 03). • When the memory button M is pressed again, you can view your individual measured values. • To switch the device off again, press the Start/stop button or wait 30 sec.
10. What if there are problems? Error message Possible cause Solution Er1 Unable to record a pulse. Er2 You moved or spoke during the measure ment. Please wait one minute and repeat the mea surement. Ensure that you do not speak or move during the measurement. Er3 The cuff is not attached correctly. Er4 The measured values are outside the speci fied measurement range. - Please observe the information in chapter „Attaching the cuff“ and take another measu rement after one minute.
• The codes below are printed on batteries containing harmful substances: Pb = Battery contains lead, Cd = Battery contains cadmium, Hg = Battery contains mercury. 12. Specifications Device Model no.
• This unit is in line with European Standard EN 60601-1-2 (i n accordance with C ISPR 11, IEC61000-3-3, IEC61000-4-2, IEC61000-4-3, IEC61000-4-4, IEC61000-4-5, IEC61000-4-6, IEC61000-4-8, IEC61000-4-11 ) and is subject to particular precautions with regard to electromagnetic compatibility (EEC). Please note that portable and mobile HF communication systems may interfere with this unit.
The following are explicitly excluded from this warranty: – deterioration due to normal use or consumption of the product; – accessories supplied with this product which are worn out or used up through proper use (e.g.
Appendix I Guidance and manufacturer’s declaration - electromagnetic emissions The Sphygmomanometer (MD6000) is intended for use in the electromagnetic environment specified below. The customer or the user of the Sphygmomanometer (MD6000) should assure that it is used in such an environment.
Appendix II Guidance and manufacturer’s declaration - electromagnetic Immunity The Sphygmomanometer (MD6000) is intended for use in the electromagnetic environment specified below. The customer or the user of the Sphygmomanometer (MD6000) should assure that it is used in such an environment.
Appendix III Guidance and manufacturer’s declaration - electromagnetic Immunity The Sphygmomanometer (MD6000) is intended for use in the electromagnetic environment specified below. The customer or the user of the Sphygmomanometer (MD6000) should assure that it is used in such an environment.
Appendix IV Recommended separation distances between portable and mobile RF communications equipment and the Sphygmomanometer (MD6000) The Sphygmomanometer (MD6000) is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
Appendix V 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. NOTE: 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.
Appendix VI Instructions for use The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments and so on. Warning：Don’t near active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high. Warning： Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation.
Symbol for the marking of electrical and electronics devices according to Directive 2002/96/EC. The device, accessories and the packaging have to be disposed of waste correctly at the end of the usage. Please follow Local Ordinances or Regulations for disposal. Grandway Technology (Shenzhen) Limited No. 5, the Second Industrial Zone, Zhukeng Community, Longtian Street, Pingshan District, Shenzhen, 518118 The People’s Republic of China Shanghai International Holding Corp.
