ENGLISH Read these instructions for use carefully. Observe the warnings and safety notes. Keep these instructions for use for future reference. Make the instructions for use accessible to other users. If the device is passed on, provide the instructions for use to the next user as well.
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Disposal in accordance with the Waste Elec- Separate the product and packaging elements trical and Electronic Equipment EC Directive and dispose of them in accordance with local – WEEE regulations. Protected against solid foreign objects IP20 12.5 mm in diameter and larger Do not dispose of batteries containing harmful substances with household waste Direct current...
2. INTENDED USE Temperature range Intented purpose The blood pressure monitor (hereinafter, device) is intended for the fully automatic, non-invasive measurement of arterial Humidity range blood pressure and pulse values on the upper arm. It is designed for self-measurement by adults in a domestic environment.
Indications Undesirable side effects In the event of hypertension or hypotension, the user can in- • skin irritation dependently monitor their blood pressure and pulse values at • negative impact on blood circulation home. However, the user does not need to be suffering from 3.
measuring device to malfunction and/or an inaccurate arrhythmia, circulatory problems, diabetes, pregnancy, measurement. pre-eclampsia, hypotension, chills, shaking • Do not use the device outside of the specified storage • To rule out a difference between sides, the measurement and operating conditions. This could lead to incorrect should initially be taken on both arms.
Notes on handling batteries Notes on electromagnetic compatibility WARNING CAUTION • If your skin or eyes come into contact with battery flu- • The device is suitable for use in all environments listed id, rinse the affected areas with water and seek medical in these instructions for use, including domestic environ- assistance.
4. INCLUDED IN DELIVERY Memory button Slider for user selection Check that the exterior of the cardboard delivery packaging Information on the display is intact and make sure that all contents are present. Before use, ensure that there is no visible damage to the device or Symbol for Bluetooth ®...
• Insert the batteries (see chapter “Technical specifica- from the blood pressure monitor. As soon as you unplug tions”). Insert the batteries, making sure the polarity is the mains part, the blood pressure monitor loses the date correct according to the label and time setting but the saved measured values are re- •...
Date 6.2 Before the blood pressure measure- The year flashes: ment • Press < / > to select the year General rules when measuring your own blood The month flashes: • Press < / > to select the month pressure The day flashes: •...
Selecting the user arm with the higher blood pressure values. Consult your doc- tor about this before starting self-measurement. This device has two users with 120 memory spaces each in • Always measure your blood pressure on the same arm. order that you can save measurements from two different •...
If necessary, re-attach the cuff after 1 minute. is displayed if the measurement could not be per- The device switches off automatically after approx. formed properly. In this case, please refer to the “Trou- 30 seconds. The value is saved to the selected or most bleshooting”...
Cardiac arrhythmia Source: Source: The device can identify heart rhythm abnormalities during the blood pressure measurement. If is displayed after The risk indicator indicates which category the recorded the measurement, this indicates that an irregularity has been blood pressure values fall into. If the measured values are in two different categories (e.g.
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While the final diagnosis of atrial fibrillation can only be made namic stability when taking the blood pressure measurement. by a medical examination, the Beurer AFIB technology of this This enables it to indicate whether the blood pressure was device enables it to be detected with a high level of accuracy.
However, certain patients suffering from cardiac arrhythmia is displayed: or chronic mental conditions may remain haemodynamical- The average value of the morning measurements for the last ly unstable even in the long-term, something which persists 7 days is displayed (morning: 5:00–9:00). even after repeated periods of rest.
• Start the app. 8. ACCESSORIES AND • Select BM 64 in the app and follow the instructions. • A PIN code is displayed on the device when connecting REPLACEMENT PARTS for the first time. Enter the PIN code on the smartphone.
Designation Item number and/ Error Possible Solution or order number message cause Universal cuff 164.503 An error oc- Please wait one minute and curred during repeat the measurement. Mains adapter (EU) 072.78 the measure- Ensure that you do not Mains adapter (UK) 072.79 ment.
11. TECHNICAL SPECIFICATIONS Repairing and disposing of the device • Do not repair or modify the device yourself. Proper oper- Type BM 64 ation can no longer be guaranteed in this case. Meas- Oscillometric, non-invasive blood pressure • Do not open the device except for the battery compart-...
Input 100 – 240 V, 50 – 60 Hz, 0.5 A max tion continuous operation, type BF applied part Output 5 V DC, 1 A, in conjunction with Beurer ® Data The device uses Bluetooth blood pressure monitors only transfer via Frequency band 2.400 –...
Insulated/protection class 2 Housing and The housing of the mains part protects users protective from touching live parts or parts that could covers be live (for example with their fingers, or with a needle or checking hook). The user must not touch the patient and the output connector of the AC/DC mains part at the same time.
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The Bluetooth ® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by Beurer GmbH is under license. Other trademarks and trade names are those of their respective owners. Apple and the Apple logo are trademarks of Apple Inc., registered in the U.S. and other countries. App Store is a service mark of Apple Inc., registered in the U.S.
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