Beurer BM 40 - Manual (Page 22)

22
• 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
method Oscillometric, non-invasive blood pressure
measurement on the upper arm
Measurement
range Cuff pressure 0 – 300 mmHg,
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
inaccuracy Max. permissible standard deviation
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. 257 g (without batteries)
Cuff size 22 to 35 cm
Permissible oper-
ating conditions + 10 °C to + 40 °C, ≤ 85 % relative air humidity
(non-condensing)
Permissible stor-
age conditions - 20 °C to + 55 °C, ≤85 % relative air humidity,
800 –1060 hPa ambient pressure
Power supply 4 x 1,5 V AA batteries
Battery life For approx. 250 measurements, depending
on the blood pressure level and/or pump
pressure
Accessories Instruction for use, 4 x 1.5 V AA batteries,
storage pouch
Classification Internal supply, IPX0, no AP or APG, con-
tinuous operation, type BF applied part
Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601-1-2 and
is subject to particular precautions with regard to electro-
magnetic compatibility (EMC). Please note that portable and
mobile HF communication systems may interfere with this
unit. More details can be requested from the stated Customer
Service address or found at the end of the instructions for use.
• This device is in line with the EU Medical Devices Directive
93/42/EC, the „Medizinproduktegesetz“ (German Medical De-
vices Act) and the standards EN 1060-1 (non-invasive sphyg-
momanometers, Part 1: General requirements), EN 1060-3
(non-invasive sphygmomanometers, Part 3: Supplemen-
tary requirements for electro-mechanical blood pressure
measuring systems) and IEC 80601-2-30 (Medical electrical
equipment – Part 2 – 30: Particular requirements for the safety
and essential performance of automated non-invasive blood
pressure monitors).
• The accuracy of this blood pressure monitor has been care-
fully checked and developed with regard to a long useful
life. If using the device for commercial medical purposes, it