G Blood Pressure Monitor; Instructions For Use - Sanitas SBC 21 Mode D'emploi

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  • FRANÇAIS, page 21
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 70 mm x W 72 mm x H 27.5 mm
Weight
Approximately 105 g (without batteries)
Cuff size
135 to 195 mm
Permissible operat-
+10 °C to +40 °C, 30-85 % relative hu-
ing conditions
midity (non-condensing)
Permissible storage
-20 °C to +60 °C, 10-95 % relative hu-
conditions
midity, 700-1050 hPa ambient pressure
Power supply
2 x 1.5 V
Battery life
For approx. 300 measurements,
depending on levels of blood pressure
and pump pressure
Accessories
Instructions for use, 2 x 1.5 V AAA bat-
teries, storage box
Classification
Internal supply, IPX0, no AP or APG,
continuous operation, application part
type BF
• 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
All manuals and user guides at all-guides.com
AAA batteries
unit. More details can be requested from the stated Customer
Services address or found at the end of the instructions for
use.
• This device is in line with the EU Medical Devices Direc-
tive 93/42/EC, 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, Part3: 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
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 must
be regularly tested for accuracy by appropriate means. Pre-
cise instructions for checking accuracy may be requested
from the service address.
20

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