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 Medi
cal Devices Act) and the standards EN 10601 (noninva
sive sphygmomanometers, Part 1: General requirements),
EN 10603 (noninvasive sphygmomanometers, Part 3: Sup
plementary requirements for electromechanical blood pres
sure measuring systems) and IEC 80601230 (Medical elec
trical 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 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.
8194049/01
Input
100240 V, 50/60 Hz
Output
12 V DC, 600 mA, only in connection with
beurer blood pressure monitor
Supplier
Ansmann AG
Protection
This device is double insulated and pro
tected against short circuit and overload
by a primary thermal fuse.
The green LED lights under normal con
ditions.
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 and
Equipment enclosed to protect against
Protective Covers
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 DC mains part
simultaneously.
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