Beurer BC 51 Mode D'emploi page 49

Permissible operating
conditions
Permissible storage and
transport conditions
Power supply
Battery life
Classification
The serial number is located on the device or in the battery compartment.
Technical information is subject to change without notification to allow for updates.
• This device complies with the European standard EN 60601-1-2 (in compliance with CISPR 11,
IEC 61000-4-2, IEC 61000-4-3, IEC 61000-4-8) and is subject to special precautionary measures
with regard to electromagnetic compatibility. Please note that portable and mobile HF communi-
cation systems may interfere with this device.
• This device complies with the EU Medical Devices Directive 93/42/EEC, the German Medical De-
vices Act (Medizinproduktgesetz) and the standards EN 1060-1 (Non-invasive sphygmomanom-
eters – Part 1: General requirements), EN 1060-3 (Non-invasive sphygmomanometers – Part 3:
Supplementary requirements for electro-mechanical blood pressure measuring systems) and
IEC 80601-2-30 (Medical electrical equipment – Part 2-30: Particular requirements for the basic
safety and essential performance of automated non-invasive sphygmomanometers).
• The accuracy of the blood pressure monitor has been carefully checked. No calibration is required.
• The device has been developed with regard to a long useful life. The expected operating life is
5 years.
+10°C to +40°C, < 85% relative humidity (non-condensing),
700 –1060 hPa ambient pressure
-20°C to +50°C,
< 85% relative humidity
2 x 1.5 V AAA batteries
For approx. 300 measurements, depending on levels of blood pressure
and inflation pressure
Internal supply, IP22, no AP or APG, continuous operation, application
part type BF
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