Specifications - Beurer BM 40 onpack Mode D'emploi

3: The cuff is fastened too tightly or loosely,
•
4: The pump pressure is higher than 300 mmHg,
•
5: There is a system or unit error.
•
In the above cases, you must repeat the measurement. Make sure
that the cuff tube is properly inserted and that you do not move or
talk. Re-insert the batteries if necessary, or else replace them.

10. Specifications

Model no. BM 40
Measurement Oscillometric, non-invasive blood pressure
method measurement on the upper arm
Measurement Cuff pressure 0 – 300 mmHg,
range systolic 60 – 280 mmHg,
diastolic 30 – 200 mmHg,
Pulse 30 –180 beats/minute
Display accuracy Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Measurement Max. permissible standard deviation
inaccuracy according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
Memory 2 x 60 memory spaces
Dimensions L 119 mm x W 109 mm x H 60 mm
Weight Approx. 387 g (without batteries, with cuff)
Cuff size 22 to 35 cm
Permissible oper- + 10 °C to + 40 °C, 20-90% relative air humid-
ating conditions ity (non-condensing)
Permissible stor- - 25 °C to + 55 °C, 20-90 % relative air humid-
age conditions ity, 700 –1060 hPa ambient pressure
Power supply
4 x 1,5 V
Battery life For approx. 250 measurements, depending
on the blood pressure level and/or pump
pressure
Classification Internal supply, continuous operation, type
BF applied part, IP20, no AP or APG
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, IEC61000-3-2, IEC61000-3-3,
IEC61000-4-2, IEC61000-4-3, IEC61000-4-4, IEC61000-4-5,
IEC61000-4-6, IEC61000-4-8, IEC61000-4-11) and is subject
to particular precautions with regard to electromagnetic
compatibility (EMC). Please note that portable and mobile HF
communication systems may interfere with this unit.
• This device is in line with the EU Medical Devices Directive
93/42/EEC, the „Medizinproduktegesetz" (German Medical
Devices Act) and the standards EN 1060-1 (non-invasive
sphygmomanometers, Part 1: General requirements),
EN 1060-3 (non-invasive sphygmomanometers, Part 3: Sup-
plementary requirements for electro-mechanical blood pres-
sure measuring systems) and IEC 80601-2-30 (Medical elec-
trical equipment – Part 2 – 30: Particular requirements for the
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AA batteries