Soehnle Systo Monitor 180 Mode D'emploi page 19

IMPORTANT INFORMATION! PLEASE KEEP!
Carefully read these user instructions and in particular
the safety information prior to using this device and keep
these user instructions for future use. When handing the device
over to third parties, please also include these user instructions.
Non-compliance with these instructions may cause injuries or
damage the device.
Information on use
• The device is intended for the
independent measurement and
monitoring of arterial blood pres-
sure. Only a medical doctor can
provide a diagnosis.
• The user must review the functio-
nality and proper condition of the
device prior to using it. Continued
use of a damaged device may result
in injuries and erroneous measure-
ment results or pose a serious risk.
In case of technical problems with
the device, please contact Soehnle's
CUSTOMER SERVICE. Never open or
repair the device.
• The device is intended to be used
only by adults. Do not use the de-
vice if you are pregnant or suspect
a pregnancy.
• This device may be used only for
the purpose described in these
instructions. The manufacturer
does not accept any liability for
damages based on improper use.
• The device is designed only for
personal use.
• It must not be used on any extre-
mities but the arms.
• If you take medication please ask
your doctor about the best time to
measure your blood pressure.
• If the device is used for measure-
ments on patients with widespread
arrhythmia, e.g. extrasystoles of the
atrium or ventricularextrasystoles,
the best results are generally achie-
ved with deviations. Please discuss
the results with your doctor.
• If the cuff pressure is higher than
40 kPa (300 mmHg), the device re-
leases air automatically. If the cuff
does not release air at a pressure of
40 kPa (300 mmHg), please remove
the cuff from your arm and push
the START/STOP key to prevent
further inflation.
• The device is not approved for AP
or APG categories.
• Avoid interference signals emitted
by strong electromagnetic fields
or rapid transient disturbances to
prevent measuring errors.
• The device is not suited for conti-
nuous blood pressure monitoring
in medical emergencies. Blood
circulation may be disrupted.
• The cuff material has been tested
and is proven to correspond to the
requirements of ISO 10993-5:2009
and ISO 10993-10:2010. It does
not cause skin irritation or other
reactions.
• Please use only the ACCESSORIES
and removable parts prescribed by
INTRODUCTION
GB
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