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Siare Morpheus Series - Warnings, Cautions and Notes

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VI MORPHEUS MRI
Warnings, cautions and notes
You are advised to carefully read the information given alongside the three
symbols shown on the previous page, since it contains considerations on
the saf
ety, the special requirements for the use MORPHEUS anaesthesia
unit and the relative safety regulations.
In order to understand how the MORPHEUS anaesthesia unit works
and how to use it correctly to ensure patient and user safety, the
recommendations and i
nstructions contained in this manual must be
read with care and understood.
The anaesthesia unit must only be used for the purposes specified
herein and the safety of the equipment is therefore only guaranteed if it
is used in accordance with the instructions given in this User’s Manual.
The materials used were carefully selected during the design stage after
specific checks, tests and comparative trials: these materials are also
constantly inspected during the production cycle to achieve the best
results i
n terms of reliability and safety for the patient and the operator.
Any part of circuit must therefore only be replaced with original spare
parts supplied or checked by SIARE.
The anaesthesia unit must only be used by qualified personnel and only
in equipp
ed and dedicated rooms, according to the regulations in force
in the country where the equipment is installed.
To ensure correct technical assistance and avoid possible physical
damage to the patient, the maintenance schedule foreseen in this
manual must b
e respected; qualified personnel must only carry out
maintenance of the anaesthesia unit or authorised modifications to the
equipment. The user of this product is solely responsible for any
operating defect caused by improper use or interventions carried o
ut by
third parties other than specialised SIARE personnel.
For any repairs to anaesthesia unit (due to malfunctioning, defects or
failures), the user must contact SIARE or the authorised local Technical
Service Centre; it is advisable to specify the data
on the identification
label (model, serial number, ……) when requesting intervention.
SIARE recommends establishing a maintenance and service contract
with SIARE or the local authorised service dealer in order to guarantee
the scheduled maintenance required
to operate the anaesthesia unit in
a safe and correct manner.

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