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Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601-1-2
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 1060-1 (non-invasive
sphygmomanometers, 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 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 means.
Precise instructions for checking accuracy may be requested
from the service address.

12. Mains part

Model no.
FW 7575M/EU/6/06
Input
100 – 240 V, 50 – 60 Hz
Output
Supplier
Protection
Enclosures and
Protective Covers
32
6 V DC, 600 mA, only in connection with
beurer blood pressure monitor.
Friwo Gerätebau GmbH
This device is double insulated and
protected against short circuit and
overload by a primary thermal fuse.
Make sure to take the batteries out
of the compartment before using the
mains part.
Polarity of the the DC voltage connec-
tion
Double insulated / equipment class 2
Equipment enclosed to protect against
contact with live parts, and with parts
which can become live (finger, pin,
hook test).
The operator shall not contact the pa-
tient and the output plug of AC mains
part simultaneously.
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