Beurer BM 45, Instructions For Use Manual

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The serial number is located on the device or in the battery
compartment.
Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601-1-2 (In
accordance with CISPR 11, IEC 61000-4-2, IEC 61000-4-3,
IEC 61000-4-6 and IEC 61000-4-8) and is subject to particu-
lar precautions with regard to electromagnetic compatibility
(EMC). Please note that portable and mobile HF communica-
tion systems may interfere with this unit.
• This device complies with the EU Medical Devices Directive
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 230: 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 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.
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 pri-
mary-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
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/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.