Beurer BM 85 - Manual (Page 34)

34
Technical information is subject to change without notification
to allow for updates.
• 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 Directive
93/42/EC, the German Medical Devices Act (Medizinproduk-
tgesetz) and the standards EN 1060-1 (non-invasive sphyg-
momanometers, Part 1: General requirements), EN 1060-3
(non-invasive sphygmomanometers, Part 3: Supplementary
requirements for electro-mechanical blood pressure measur-
ing systems) and IEC 80601-2-30 (Medical electrical equip-
ment – 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 R&TTE Directive 1999/5/EC.
Please contact the specified service address to obtain fur-
ther 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-
turer
Dongguan Oriental Hero Ele. Co., LTD.
Protection The device is double protected and has a pri-
mary-side cutout switch which disconnects the
device from the mains in case of malfunction.
Polarity of the the DC voltage connection
Insulated / protection class 2
Housing and
protective
covers
The housing of the mains part protects users
from touching live parts or parts that could be
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.