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User's Manual, DU3310103-MRI / rev. 3 - 02.05.2019
Year of manufacture
Check the identification data label of the equipment in the relative chapter.
Manufacturer
SIARE ENGINEERING INTERNATIONAL GROUP s.r.l.
Via Giulio Pastore , 18 - Località Crespellano,
40053 Valsamoggia (Bologna), ITALY
Tel.: +39 051 969802 - Fax: +39 051 969366
E-mail: mail@siare.it - Web: www.siare.it
Electromagnetic Compatibility
The MORPHEUS anaesthesia unit is designed to operate in the specified
electromagnetic environment (see warning below).
The customer or the user of MORPHEUS anaesthesia unit should ensure that
it is used in such an electromagnetic environment.
The MORPHEUS anaesthesia unit complies with the EN 60601-
1-2 regulations on Electromagnetic Compatibility of electro-
medical equipment. It is in any case highly recommended not to
use the anaesthesia unit adjacent to high-powered equipment
or to units, which emit strong electro-magnetic fields. Mobile
phones, cordless phones or other radio transmitters used in the
vicinity of the equipment could influence its operation.
Whenever the anaesthesia unit should be necessarily used
nearby to such equipment, it will be required to supervise its
normal operation.
In general, as regards the regulations regarding
"electromagnetic emissions", "electromagnetic immunity"
and "recommended separation distances between portable
and mobile RF equipment and the device", always refer to
what is described in the MORPHEUS anaesthesia unit user's
manual.
Requirements applicable to cables, transducers and other
ACCESSORIES
requirements of 6.1 and 6.2
that
could
affect
compliance
with
the
XI
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