Beurer BM 65: Technical information is subject to change without notifica- tion to allow for updates.
Technical information is subject to change without notifica- tion to allow for updates.: Beurer BM 65
Table of contents
- 2. Important information Signs and symbols 1. Getting to know your instrument
- Advice on use
- Storage and Care Advice on batteries
- 3. Unit description Repair and disposal
- Icons in the display: System requirements for the Beurer “Health Manager” computer software 1. Supported operating systems: 2. Supported architectures: 3. Hardware requirements:
- 4. Prepare measurement Setting date and time Inserting battery Operation with the mains part
- 5. Measuring blood pressure Positioning cuff
- Correct posture Measuring blood pressure
- 6. Evaluating results Cardiac arrhythmia: WHO classification: Range of blood pressure values Systolic
- 8. Error messages/trouble-shooting 7. Saving, retrieving and deleting results
- 10. Specifications Technical alarm – description 9. Cleaning and storing the instrument
- Technical information is subject to change without notifica- tion to allow for updates.
- 11. Adapter

nometers, Part 3: Supplementary requirements for
Power supply
4 x 1,5 V
AAA batteries
electro-mechanical blood pressure measuring systems)
Battery life For approx. 220 measurements, de-
and IEC80601-2-30 (Medical electrical equipment –
pending on the blood pressure level
Part 2 – 30: Particular requirements for the safety and
and/or pump pressure
essential performance of automated non-invasive blood
Accessories Instruction for use, 4 x 1.5 V AAA bat-
pressure monitors).
teries, storage pouch
•
The accuracy of this blood pressure monitor has been
Classification Internal supply, IPX0, no AP or APG,
carefully checked and developed with regard to a long
continuous operation, type BF applied
useful life. If using the device for commercial medical pur-
part
poses, it must be regularly tested for accuracy by appro-
priate means. Precise instructions for checking accuracy
Technical information is subject to change without notifica-
may be requested from the service address.
tion to allow for updates.
•
This unit is in line with European Standard EN 60601-1-2
and is subject to particular precautions with regard to
electromagnetic compatibility (EMC). Please note that
portable and mobile HF communication systems may in-
terfere with this unit. More details can be requested from
the stated Customer Service address or found at the end
of the instructions for use.
•
This device is in line with the EU Medical Devices Direc-
tive 93/42/EC, the „Medizinproduktegesetz“ (German
Medical Devices Act) and the standards EN1060-1
(non-invasive sphygmomanometers, Part 1: General
requirements), EN1060-3 (non-invasive sphygmoma-
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