Technical Specifications - Beurer BM 35 Mode D'emploi

4. the cuff tube is not inserted properly
5. the cuff is inflated for longer than 25 seconds
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. Technical Specifications

Type: BM 35/1
Model no. BM 35
Measurement Oscillometric, non-invasive blood pres-
method sure measurement on the upper arm
Measurement range Cuff pressure 0 – 300 mmHg,
systolic 60 – 280 mmHg,
diastolic 30 – 200 mmHg,
Pulse 40 – 199 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 135 mm x W 105 mm x H 53 mm
Weight Approx. 327 g (without batteries)
Cuff size 22 to 36 cm
Permissible operating +5 °C to +40 °C, 15-93 % relative air
conditions humidity (non-condensing)
,
Permissible storage
.
conditions
Power supply
Battery life
Classification
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
• This device is in line with the EU Medical Devices Directive
23
-25 °C to +70 °C, ≤ 93 % relative air
humidity, 860 –1060 hPa ambient
pressure
4 x 1,5 V
For approx. 250 measurements,
depending on the blood pressure level
and/or pump pressure
Internal supply, IPX0, no AP or APG,
continuous operation, type BF applied
part
accordance with CISPR 11, IEC 61000-4-2, IEC 61000-4-3
and IEC 61000-4-8) 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.
93/42/EEC, the „Medizinproduktegesetz" (German Medi-
cal Devices Act) and the standards EN 1060-1 (non-inva-
sive 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
AAA batteries