Sanitas SBC 24 Mode D'emploi page 19

Display accuracy Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Measurement Max. permissible standard deviation accord-
inaccuracy ing to clinical testing: systolic 8 mmHg /
diastolic 8 mmHg
Memory 60 memory spaces
Dimensions L 94,8 mm x W 63,3 mm x H 25,5 mm
Weight Approx. 103 g (without batteries)
Cuff size 140 to 195 mm
Permissible operating +10 °C to +40 °C, ≤ 85 % relative air humidity
conditions (non-condensing)
Permissible storage -20 °C to +50 °C, ≤ 85 % relative air humidity,
conditions 800 –1050 hPa ambient pressure
Power supply
2 x 1,5 V
Battery life For approx. 270 measurements, depending
on the blood pressure level and/or pump
pressure
Accessories Instruction for use, 2 x 1.5 V AAA batteries,
protective cover for display
Classification Internal supply, IPX0, no AP or APG, continu-
ous operation, type BF applied part
All manuals and user guides at all-guides.com
AAA batteries
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 electromagnetic
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 Devices Act)
and the standards EN 1060-1 (non-invasive sphygmomanometers,
Part 1: General requirements), EN 1060-3 (non-invasive sphyg-
momanometers, Part 3: Supplementary 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 carefully
checked and developed with regard to a long useful life. If using the
device for commercial medical purposes, it must be regularly tested
for accuracy by appropriate means. Precise instructions for checking
accuracy may be requested from the se rvice address.
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