Beurer BM 85: Technical information is subject to change without notification 3. Mains part to allow for updates.

Technical information is subject to change without notification

1

3. Mains part

to allow for updates.

Model No. OH-1048A0500600U2 VDE

•

This device complies with European Standard EN60601-

Input 100 – 240 V AC, 50 – 60 Hz; 120-60 mA

1-2 and is subject to particular precautions with regard to

Output 5 V DC, 600 mA, in conjunction with Beurer

electromagnetic compatibility. Please note that portable and

blood pressure monitors only

mobile HF communication systems may interfere with this

Manufac-

Dongguan Oriental Hero Ele. Co., LTD.

unit. More details can be requested from the stated Custom-

turer

er Services address or found at the end of the instructions

for use.

Protection The device is double protected and has a pri-

•

This device corresponds to the EU Medical Devices Directive

mary-side cutout switch which disconnects the

93/42/EC, the German Medical Devices Act (Medizinproduk-

device from the mains in case of malfunction.

tgesetz) and the standards EN1060-1 (non-invasive sphyg-

Polarity of the the DC voltage connection

momanometers, Part 1: General requirements), EN1060-3

(non-invasive sphygmomanometers, Part 3: Supplementary

Insulated / protection class 2

requirements for electro-mechanical blood pressure measur-

Housing and

The housing of the mains part protects users

ing systems) and IEC80601-2-30 (Medical electrical equip-

protective

from touching live parts or parts that could be

ment – Part 2 – 30: Particular requirements for the basic

covers

live (for example with their fingers, or with a

safety and essential performance of automated non-invasive

needle or checking hook).

sphygmomanometers).

The user must not touch the patient and the

•

The accuracy of this blood pressure monitor has been care-

output connector of the AC mains part at the

fully checked and developed with regard to a long useful

same time.

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.

34