Manual
49
Permissible operating
conditions
+10°C to +40°C, < 85% relative humidity (non-condensing),
700–1060 hPa ambient pressure
Permissible storage and
transport conditions
-20°C to +50°C,
< 85% relative humidity
Power supply 2 x 1.5 V
AAA batteries
Battery life For approx. 300 measurements, depending on levels of blood pressure
and inflation pressure
Classification Internal supply, IP22, no AP or APG, continuous operation, application
part type BF
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.
•
T
his device complies with the European standard EN60601-1-2 (in compliance with CISPR 11,
IEC 61000-4-2, IEC61000-4-3, IEC61000-4-8) 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.
•
T
his device complies with the EU Medical Devices Directive 93/42/EEC, the German Medical De-
vices Act (Medizinproduktgesetz) and the standards EN1060-1 (Non-invasive sphygmomanom-
eters – Part1: General requirements), EN1060-3 (Non-invasive sphygmomanometers – Part3:
Supplementary requirements for electro-mechanical blood pressure measuring systems) and
IEC80601-2-30 (Medical electrical equipment – Part2-30: Particular requirements for the basic
safety and essential performance of automated non-invasive sphygmomanometers).
•
T
he accuracy of the blood pressure monitor has been carefully checked. No calibration is required.
•
T
he device has been developed with regard to a long useful life. The expected operating life is
5 years.