Beurer BM 58 User Manual download pdf (Page 29)

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This unit is in line with European Standard EN 60601-1-2

and is subject to particular precautions with regard to

electromagnetic compatibility (EMC). Please note that

portable and mobile HF communication systems may

interfere with this unit. More details can be requested

from the stated Customer Service address or found at the

end of the instructions for use.

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This device is in line with the EU Medical Devices Direc-

tive 93/42/EC, the „Medizinproduktegesetz“ (German

Medical Devices Act) and the standards EN1060-1

(non-invasive sphygmomanometers, Part 1: General

requirements), EN1060-3 (non-invasive sphygmoma-

nometers, Part 3: Supplementary requirements for elec-

tro-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).

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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.

12. 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.

Double insulated / equipment class 2

Polarity of the the DC voltage con-

nection

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 mains

part simultaneously.

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