Beurer BM 58 - Manual (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.
• 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).
• 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.