User Manual for the FLUXMEDICARE® V2 System
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IFU-FLUXMEDV2 - V.1.0 - 07/2020
Page 37 / 84
2.
Warnings, symbols
2.1.
Warnings and safety remarks
This manual contains several warnings describing the banning of or the obligation for certain actions required
on the part of the user in order to operate the system in complete safety.
In this manual the warnings are notified by a pictogram
(exclamation mark within a yellow triangle).
Non-
adherence to these directions for use may lead to serious injury, to the patient and/or the user!
In this manual the information is notified by a pictogram
(the letter “i” contained in a blue circle).
The following warnings should be read carefully!
CAUTION:
•
Do not use the device before reading the user manual carefully and understanding it.
•
Do not use electrical power outside the nominal limits specified in the user manual or
printed on the back of the device.
•
Risk of eye injuries. Check that safety instructions and principles are followed, and
there is no possibility of direct light transmission outside the application area.
•
Do not look directly at the light emitted.
•
Any opening of equipment requiring a tool is only authorised for MDB Texinov
personnel.
•
Modifying the FLUXMEDICARE® V2 system is PROHIBITED.
•
Do not use for indications other than those specified in this document.
•
Risk of eye injuries. Do not leave the light fibres illuminated when these are not being
applied to the patient.
•
Do not connect accessories other than those specified.
•
Do not obstruct the air vents, or place the appliance on a soft or sloping surface.
•
Adhere to a free space or a distance from the wall of at least 30 cm on all ventilation
faces.
•
Do not use an electrical extension lead.
•
Only use the count key supplied.
•
Do not connect another appliance or count connector (USB type) on the front face of
the light source.
•
Do not connect this key to a computer or any other electronic appliance.
•
Do not place the source on an unstable surface.
•
In order to prevent the risk of electric shock, the FLUXMEDICARE® V2 device must be
connected to an electric socket with earthing protection.
•
The source must not come into contact with a liquid.
•
The FLUXMEDICARE® V2 system must not be exposed to high pressures or pointed
objects.
•
The current socket plug is the disconnection device and should remain accessible.
•
Do not use beyond the duration for use.
•
In the treatment room, avoid storing and using flammable materials such as oxygen
and some anaesthetics.
2.2.
Safety linked to the light device
Any fault deactivates the light emission.
If the connector disconnects, the light stops, the source emits a sound signal and the treatment is stopped.