Cleaning And Storing The Device And Cuff; Technical Details - Beurer BC 30 Mode D'emploi

8. Cleaning and storing the device and cuff

• Clean the device and cuff carefully using a slightly damp
cloth only.
• Do not use any cleaning agents or solvents.
• Under no circumstances hold the device and cuff under
water, as this can cause liquid to enter and damage the
device and cuff.
• If you store the device and cuff, do not place heavy objects
on the device and cuff. Remove the batteries.

9. Technical details

Model no. BC 30
Measurement Oscillometric, non-invasive blood pressure
method measurement on the wrist
Measurement Cuff pressure 0 – 300 mmHg,
range systolic 40 – 280 mmHg,
diastolic 40 – 280 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 3 x 40 memory spaces
Dimensions L 70 mm x W 72 mm x H 28,6 mm
Weight Approx. 112 g (without batteries)
Cuff size 135 to 195 mm
All manuals and user guides at all-guides.com
Permissible oper- + 5 °C to +40 °C, 15 – 93 % relative air
ating conditions humidity (non-condensing)
Permissible stor- -25 °C to +70 °C, ≤ 93 % relative air humid-
age conditions ity, 700 –1060 hPa ambient
pressure
Power supply
2 x 1,5 V
Battery life For approx. 250 measurements, depending
on the blood pressure level and/or pump
pressure
Accessories Instruction for use, 2 x 1.5 V AAA batteries,
storage box
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 elec-
tromagnetic compatibility (EMC). Please note that portable
and mobile HF communication systems may interfere with
this unit. More details can be requested from the stated Cus-
tomer 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/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-
21
AAA batteries