Instructions For Use - Beurer medical BM 20 Gebrauchsanweisung

Enclosures and Equipment enclosed to protect against
Protective Covers contact with live parts, and with parts
which can become live (finger, pin, hook
test).
The operator shall not contact the patient
and the output plug of AC mains part
simultaneously.
• 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 port­
able and mobile HF communication systems may inter­
fere 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 Directive
93/42/EEC, the „Medizinproduktegesetz" (German Medi­
cal Devices Act) and the standards EN 1060­1 (non­inva­
sive sphygmomanometers, Part 1: General requirements),
EN 1060­3 (non­invasive sphygmomanometers, Part 3:
Supplementary requirements for electro­mechanical blood
pressure measuring systems) and IEC 80601­2­30 (Medical
electrical equipment – Part 2 – 30: Particular requirements
for the safety and essential performance of automated non­
invasive 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
All manuals and user guides at all-guides.com
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means. Precise instructions for checking accuracy may be
requested from the service address.