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Mains Part - Beurer BM 44 Gebrauchsanweisung

Vorschau ausblenden Andere Handbücher für BM 44:
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Technical information is subject to change without notifica­
tion to allow for updates.
• This unit is in line with European Standard EN 60601­1­2
and is subject to particular precautions with regard to
electromagnetic compatibility (EMC). Please note that
portable and mobile HF communication systems may in­
terfere 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 Direc­
tive 93/42/EEC, the "Medizinproduktegesetz" (German
Medical Devices Act) and the standards EN 1060­1
(non­invasive sphygmomanometers, Part 1: General
requirements), EN 1060­3 (non­invasive sphygmoma­
nometers, 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 non­invasive blood
pressure monitors).
• The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life. If using the device for commercial medical pur­
poses, it must be regularly tested for accuracy by appro­
priate means. Precise instructions for checking accuracy
may be requested from the service address.

9. Mains part

Model no.
FW 7575M/EU/6/06
Input
100 – 240 V, 50 – 60 Hz
Output
6 V DC, 600 mA, in connection with Beurer
blood pressure monitor
Supplier
Friwo Gerätebau GmbH
Protection
This device is double insulated and pro­
tected 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.
double insulated / equipment class 2
Polarity of the the DC voltage connection
Enclosures
Equipment enclosed to protect against
and Protective
contact with live parts, and with parts which
Covers
can become live (finger, pin, hook test).
The operator shall not contact the patient
and the output plug of AC mains part simul­
taneously.
25

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