Seca 665 Mode D'emploi page 57

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CAUTION!
Patient hazard, damage to device
Additional devices which are connected to
electrical medical devices must provide evi-
dence of compliance with the relevant IEC or
ISO standards (e.g. IEC 60950 for data-pro-
cessing devices). Furthermore, all configura-
tions must comply with the requirements of
standards for medical systems (see IEC
60601-1-1 or Section 16 of the 3rd edition of
IEC 60601-1 respectively). Anyone connect-
ing additional devices to electrical medical
devices is considered a system configurer
and is therefore responsible for ensuring that
the system complies with the requirements of
standards for systems. Your attention is
drawn to the fact that local laws take prece-
dence over the above-mentioned require-
ments of standards. In the event of any
queries, please contact your local specialist
dealer or Technical Service.
Have servicing and recalibration carried out
regularly as described in the relevant section
of this document.
Technical modifications may not be made to
the device. The device does not contain any
parts for servicing by the user. Only have ser-
vicing and repairs performed by an autho-
rized seca service partner. You can find
service partners in your area at www.se-
ca.com or by sending an e-mail to ser-
vice@seca.com.
Only use original seca accessories and spare
parts, otherwise seca will not grant any war-
ranty.
CAUTION!
Patient hazard, malfunction
Keep other electrical medical devices, e.g.
high-frequency surgical devices, a minimum
distance of approx. 1 meter away to prevent
incorrect measurements or wireless trans-
mission interference.
Keep HF devices such as cell phones a mini-
mum distance of approx. 1 meter away to
prevent incorrect measurements or wireless
transmission interference.
English
Safety information • 57

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