Related Manuals for Beurer BM 81 easyLock
Summary of Contents for Beurer BM 81 easyLock
- Page 1 Model: MD6000 BM 81 easyLock EN Upper arm blood pressure monitor Instructions for use...
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Page 2: Table Of Contents
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 .......... - Page 3 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...
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Page 4: Intended Use
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. Target group It is designed for self-measurement by adults in the home environment and is suitable for users whose upper Indication/clinical benefits... - Page 5 • 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 speci ed storage and operating conditions. This could lead to incorrect measurements.
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Page 6: Device Description
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. -
Page 7: Initial Use
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. •... -
Page 8: Usage
If the hour format is set as 12h, the day/month display sequence is reversed. The hour ashes on the display . • Using the +/- setting buttons, select your desired number for the hour and con rm with the M memory button. The minute ashes on the display . - Page 9 • T with your upper arm circumference. The fit should be checked before measurement using the index mark described below. Ref. no. Designation Arm c ircumference 164.290* easyLock- Universal cu 24-40 cm * Included in standard delivery • P The circulation of the arm must not be hindered by tight clothing or similar.
- Page 10 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. •...
- Page 11 Bluetooth low energy technology. ® For this you need the “beurer HealthManager Pro” or “beurer HealthManager” app. These apps are available for free in the Apple App Store and from Google Play. System requirements: – iOS ≥ 12.0, Android ≥...
- Page 12 Also note the following information: • E nsure that the „beurer HealthManager Pro“ or „beurer HealthManager“ app on your smartphone is always activated and open when you start the data transfer on the device. • You can tell that the data transfer is in progress by the Bluetooth symbol shown on the display.
- Page 13 LED risk indicator The World Health Organization (WHO) has de ned the internationally recognised classi cation for the evalua- tion of measured blood pressure values listed in the table below: Measured blood pressure value range Colour of the risk Classification indicator Systole (in mmHg) Diastole (in mmHg)
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Page 14: Cleaning And Maintenance
PM ashes 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). •... -
Page 15: What If There Are Problems
10. What if there are problems? Error Possible cause Solution message Unable to record a pulse. Please wait one minute and repeat the mea surement. You moved or spoke during the measure Ensure that you do not speak or move during ment. -
Page 16: Speci Cations
• The codes below are printed on batteries containing harmful substances: Pb = Battery contains lead, Cd = Battery contains cadmium, Hg = Battery contains mercury. 12. Speci cations Device Model no. MD6000 Type BM 81 Measurement method Oscillometric, non-invasive blood pressure measurement on the upper arm Measurement range Cu pressure 0 –... -
Page 17: Warranty / Service
During the warranty period, should this product prove to be incomplete or defective in functionality in accor dance with the following provisions, Beurer shall carry out a repair or a replacement delivery free of charge, in accordance with these warranty conditions. - Page 18 Beurer; – damage that arises during transport between manufacturer and customer, or between service centre and customer;...
- Page 19 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. Compliance Emissions test RF emissions...
- Page 20 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. Immunity test IEC 60601-1-2 Test level Compliance level...
- Page 21 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. Radiated RF Test Frequency Band...
- Page 22 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. The customer or the user of the Sphygmomanometer (MD6000) can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Sphygmomanometer (MD6000) as recommended below, according to the maximum output power of the communications equipment.
- Page 23 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.
- Page 24 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：...
- Page 25 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.