Mains Part - Beurer medical BM 57 Mode D'emploi

er Services address or found at the end of the instructions
for use.
• This device corresponds to the EU Medical Devices Directive
93/42/EEC, the German Medical Devices Act (Medizinpro-
duktgesetz) and the standards DIN EN ISO81060-1 (non-in-
vasive sphygmomanometers – Part 1: Requirements and test
methods for non-automated measurement type). EN1060-3
(non-invasive sphygmomanometers – Part 3: Supplementary
requirements for electro-mechanical blood pressure measur-
ing systems) and IEC80601-2-30 (Medical electrical equip-
ment – Part 2 – 30: Particular requirements for the basic
safety and essential performance of automated non-invasive
sphygmomanometers).
• 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.
Precise instructions for checking accuracy may be requested
from the service address.
• We hereby guarantee that this product complies with the
European R&TTE Directive 1999/5/EC.
Please contact the specified service address to obtain more
detailed information such as the CE conformity declaration.

11. Mains part

Model no. 8194047/02
Input 100 – 240 V AC, 50 – 60 Hz
Output 6 V, 600 mA, in conjunction with Beurer blood
pressure monitors only
Manufac- Ansmann AG
turer
Protection The device is double protected and has a pri-
mary-side cutout switch which disconnects the
device from the mains in case of malfunction.
Ensure that you have removed the batteries from
the battery compartment before you use the
mains part.
Insulated/protection class 2
Housing and The housing of the mains part protects users
protective from touching live parts or parts that could be
covers live (for example with finger, needle, checking
hook).
Do not touch the patient and the output connec-
tor of the AC/DC mains part at the same time.
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