
System description
80028000_030_C – 773607 – 2021-09-01
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using the system near strong electromagnetic fields;
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using the system differently from what is required in paragraph
“Intended use”.
Any other use of the system with respect to the intended use must
be previously authorized in writing by the Manufacturer. Any use
that does not comply with the conditions specified above shall be
considered “misuse”; therefore the Manufacturer declines any
liability for damage caused to things or persons and deems any
type of warranty for the system void.
Improper use of the system disclaims any liability of the
manufacturer.
4.3
Use associated with other medical devices
The Helion Video Management System can be used with medical
devices from other manufacturers. The operation of these devices
is described in the relevant operating instructions.
Only medical devices (e.g. Room Camera) compliant with IEC
standard 60601-1 can be connected to the system.
If a medical device is installed at a later date, installation must be
carried out as specified in IEC standard 60601-1. Environmental
conditions for the operation and storage of Helion must be met,
see “Technical data” paragraph.
4.4
Obligations and prohibitions
The VIDEOMED Helion system must only be used by medical and
paramedical personnel with the necessary professional
qualifications, who have read these instructions for use and who
have been adequately trained in the use of the system. The
training is certified through participation in the training course
called “training for healthcare personnel in the use of Helion”. This
training must be documented.
Содержание Helion Rack
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