Beurer BM 54 Mode D'emploi page 31

Memory 2 x 60 memory spaces
Dimensions L 139 mm x W 94 mm x H 48 mm
Weight Approx. 360 g (without batteries, with cu )
Cu size 22 to 44 cm upper arm circumference
Operating con- + 5 °C to + 40 °C, 15% – 93% relative humidity,
ditions 700 –1060 hPa ambient pressure
Storage and trans- - 25 °C to + 70 °C, ≤ 93% relative humidity (non-condens-
port conditions ing)
Power supply 4 x 1.5 V
Battery life For approx. 200 measurements depending on blood pres-
sure and inflation pressure levels as well as the number of
®
Bluetooth
Product life cycle Information on the life cycle of the product can be found
to be expected at beurer.com
Classification Internal power supply, IP 20 no AP or APG, continuous
operation
Blood pressure: Application part, type BF
Data transfer via The device uses Bluetooth
® wire- Frequency band 2402 – 2480 MHz, max. transmission
Bluetooth
less technology power 4 dBm
Compatible with Bluetooth
The serial number is located on the device or in the battery compartment.
Technical specifications are subject to change without notification to allow for
updates.
LR03 AAA batteries
connections
® ,
® 4.0 smartphones/tablets
• This device conforms with the European standard EN 60601-1-2 (Group 1,
Class B, in accordance with CISPR-11, IEC 61000-3-2, IEC 61000-3-3,
IEC 61000-4-2, IEC 61000-4-3,
IEC 61000-4-6, IEC 61000-4-7, IEC 61000-4-8, IEC 61000-4-11) and is
subject to particular precautions with regard to electromagnetic compat-
ibility. Please note that portable and mobile HF communication systems
may interfere with this device.
• 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 re-
quested from the service address.
• We hereby confirm that this product complies with the European RED Di-
rective 2014/53/EU. The CE Declaration of Conformity for this product can
be found at:
www.beurer.com/web/we-landingpages/de/cedeclarationofconformity.
php
12. GUARANTEE/SERVICE
Further information on the guarantee and guarantee conditions can be
found in the guarantee leaflet supplied.
Notification of incidents
For users/patients in the European Union and identical regulation systems
(EU Medical Device Regulation (MDR) 2017/745), the following applies: If
during or through use of the product a major incident occurs, notify the
manufacturer and/or their representative of this as well as the respective
national authority of the member state in which the user/patient is located.
31
IEC 61000-4-4, IEC 61000-4-5,