Beurer medical BC 32 Mode D'emploi page 20

Classification Internal supply, IPX0, no AP or APG,
continuous operation, type BF applied
part
Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601­1­2
and is subject to particular precautions with regard to elec­
tromagnetic compatibility (EMC). Please note that portable
and mobile HF communication systems may interfere with
this unit. More details can be requested from the stated Cus­
tomer Service address or found at the end of the instructions
for use.
• This device is in line with the EU Medical Devices Directive
93/42/EEC, the „Medizinproduktegesetz" (German Medical
Devices Act) and the standards EN 1060­1 (non­ invasive
sphygmomanometers, Part 1: General requirements),
EN 1060­3 (non­invasive sphygmomanometers, Part 3: Sup­
plementary requirements for electro­mechanical blood pres­
sure measuring systems) and IEC 80601­2­30 (Medical elec­
trical equipment – Part 2 – 30: Particular requirements for the
safety and essential performance of automated non­invasive
blood pressure monitors).
• The accuracy of this blood pressure monitor has been care­
fully checked and developed with regard to a long useful life.
If using the device for commercial medical purposes, it must
be regularly tested for accuracy by appropriate means. Pre­
cise instructions for checking accuracy may be requested
from the service address.
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