DANGER!
Risk of explosion
Do not use the device in an environment in
which one of the following gases has accumu-
lated:
– oxygen
– flammable anesthetics
– other flammable substances/air mixtures
CAUTION!
Patient hazard, damage to device
►
Additional devices which are connected to
electrical medical devices must provide
evidence of compliance with the relevant IEC
or ISO standards (e.g. IEC 60950 for data-
processing devices). Furthermore, all
configurations 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 connecting 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. This also applies to additional
devices recommended by
attention is drawn to the fact that local laws
take precedence over the above-mentioned
requirements of standards. In the event of
any queries, please contact your local
specialist dealer or Technical Service.
►
Have servicing and verification 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
servicing and repairs performed by an
authorized seca Service partner. You can find
service partners in your area at
www.seca.com or by sending an e-mail to
service@seca.com.
►
Only use original seca accessories and spare
parts, otherwise seca will not grant any
warranty.
English
seca.
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Safety information • 65