Sanitas SBC 15 Mode D'emploi page 32

Measurement inac- Max. permissible standard devia-
curacy tion according to clinical testing:
Systolic 8 mmHg /
Diastolic 8 mmHg
Memory 2 x 60 memory spaces
Dimensions L 83.8 mm x W 59.9 mm x
H 29.4 mm
Weight Approximately 92 g (without batter-
ies, with cuff)
Cuff size 140 to 195 mm
Permissible operat- + 10°C to +40°C, ≤85% relative
ing conditions humidity (non-condensing)
Permissible storage -20°C to +50 °C, ≤ 85% relative
conditions humidity, 800 – 1050 hPa ambient
pressure
Power supply
2 x 1.5V
Battery life For approx. 170 measurements,
depending on levels of blood pres-
sure and pump pressure
Classification Internal supply, IP22, no AP or
APG, continuous operation, appli-
cation part type BF
Technical information is subject to change without notifi-
cation to allow for updates.
• This device complies with European Stand-
• The device complies with the EU Medical Devices
AAA batteries
• The accuracy of this blood pressure monitor has been
32
ard EN 60601-1-2 (in accordance with CISPR 11,
EN 61000-4-2, EN 61000-4-3, EN 61000-4-8) and is
subject to particular precautions with regard to electro-
magnetic compatibility. Please note that portable and
mobile HF communication systems may interfere with
this unit.
Directive 93/42/EEC, the German Medical Devices Act
(Medizinproduktgesetz) and the standards EN 1060-1
(Non-invasive sphygmomanometers – Part 1: General
requirements), EN 1060-3 (Non-invasive sphygmoma-
nometers – Part 3: Supplementary requirements for
electro-mechanical blood pressure measuring sys-
tems) and IEC 80601-2-30 (Medical electrical equip-
ment – Part 2 – 30: Particular requirements for the
basic safety and essential performance of automated
non-invasive sphygmomanometers).
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 service address.