Mains Part - Beurer medical BM 16 Gebrauchsanweisung

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/EEC, the "Medizinproduktegesetz" (German Medi-
cal 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. 8194049/01
Input 100-240 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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