Mains Part - Beurer BM 85 Gebrauchsanweisung

• This device complies with European Standard EN60601-
1-2 and is subject to particular precautions with regard to
electromagnetic compatibility. Please note that portable and
mobile HF communication systems may interfere with this
unit. More details can be requested from the stated Custom-
er Services address or found at the end of the instructions
for use.
• This device corresponds to the EU Medical Devices Direc-
tive 93/42/EEC, the German Medical Devices Act (Medizin-
produktgesetz) and the standards EN 1060-1 (non-invasive
sphygmomanometers, Part 1: General requirements),
EN 1060-3 (non-invasive sphygmomanometers, Part 3:
Supplementary requirements for electro-mechanical blood
pressure measuring systems) and IEC 80601-2-30 (Medical
electrical equipment – Part 2 – 30: Particular requirements
for the basic safety and essential performance of automated
non-invasive sphygmomanometers).
• 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.
Precise instructions for checking accuracy may be requested
from the service address.
• We hereby guarantee that this product complies with
the European RED Directive 2014/53/EU. Please contact
kd@beurer.de to obtain detailed information, such as the CE
Declaration of Conformity.

13. Mains part

Model No. OH-1048A0500600U2 VDE
Input 100 – 240 V AC, 50 – 60 Hz; 120-60 mA
Output 5 V DC, 600 mA, in conjunction with Beurer
blood pressure monitors only
Manufac- Dongguan Oriental Hero Ele. Co., LTD.
turer
Protection The device is double protected and has a
primary-side cutout switch which discon-
nects the device from the mains in case of
malfunction.
Polarity of the the DC voltage connection
Insulated / protection class 2
Housing and The housing of the mains part protects users
protective from touching live parts or parts that could be
covers live (for example with their fingers, or with a
needle or checking hook).
The user must not touch the patient and the
output connector of the AC mains part at the
same time.
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