Beurer medical BM 19 Mode D'emploi page 22

• This device is in line with the EU Medical Devices Direc­
tive 93/42/EC, 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.
Mains part
Model­No. FW7333SM06
Input 100 – 240 V, 50 – 60 Hz
Output 6V DC, 1150 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 overload
by a primary thermal fuse.
The green LED lights under normal
conditions.
Make sure to take the batteries out of the
compartment before using the mains part.
-
Polarity of the DC voltage connection
+
Double insulated /
equipment class 2
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 AC mains
part simulta neously.
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