Warranty/Service; Mains Part - Beurer BM 49 Instrucciones De Uso

• This device complies with the European standard EN60601 1-2
(in compliance with CISPR 11, IEC 61000-4-2, IEC 61000-4-3,
IEC 61000-4-4, IEC 61000-4-5, IEC 61000-4-6, IEC 61000-4-8,
IEC 61000-4-11) and is subject to special precautionary measures with
regard to electromagnetic compatibility. Please note that portable and
mobile HF communication systems may interfere with this device.
• The device complies with the EU Medical Devices Directive 93/42/
EEC, the German Medical Devices Act (Medizinproduktgesetz) and
the standards EN1060-1 (Non-invasive sphygmomanometers – Part 1:
General requirements), EN1060-3 (Non-invasive sphygmomanometers
– Part 3: Supplementary requirements for electro-mechanical
blood pressure measuring systems) and IEC80601-2-30 (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 carefully
checked and developed with regard to a long useful life. If the device
is used 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.

12.2 Mains part

Model no. LXCP12-006060BEH
Input 100 – 240 V, 50 – 60 Hz, 0.5 A max
Output 6 V DC, 600 mA, in conjunction with Beurer blood
pressure monitors only
Manufacturer Shenzhen Iongxc power supply co., ltd.
Protection This device is double protected and has a primary-
side cutout switch which disconnects the device from
the mains in case of malfunction.
Ensure that you have removed the batteries from the
battery compartment before you use the mains part.
Polarity of the DC voltage connection
Insulated/protection class 2
Housing and pro- The housing of the mains part protects users
tective covers 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/DC mains part at the same time.

13. Warranty/service

Beurer GmbH, Söflinger Straße 218, 89077 Ulm, Germany
(hereinafter referred to as "Beurer") provides a warranty for this
product, subject to the requirements below and to the extent
described as follows.
The warranty conditions below shall not affect the seller's statutory
warranty obligations which ensue from the sales agreement with the
buyer.
The warranty shall apply without prejudice to any mandatory
statutory provisions on liability.
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