Beurer BM 60 User Manual download pdf (Page 24)

100

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/EC, the “Medizinproduktegesetz” (German Medical

Devices Act) and the standards EN1060-1 (non-inva-

sive sphygmomanometers, Part 1: General requirements),

EN1060-3 (non-invasive sphygmomanometers, Part 3: Sup-

plementary requirements for electro-mechanical blood pres-

sure measuring systems) and IEC80601-2-30 (Medical elec-

trical 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. Pre-

cise instructions for checking accuracy may be requested

from the service address.

10. Mains part

Model no. FW 7575M/EU/6/06

Input 100 – 240 V, 50 – 60 Hz

Output 6 V DC, 600 mA, only in connection with

beurer blood pressure monitor.

Supplier Friwo Gerätebau GmbH

Protection This device is double insulated and pro-

tected against short circuit and over-

load 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

Enclosures and

Protective Covers

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

patient and the output plug of AC mains

part simultaneously.

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