User Manual for the FLUXMEDICARE® V2 System
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IFU-FLUXMEDV2 - V.1.0 - 07/2020
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The system must not be stored near a heat source or in direct sunlight.
The luminous bands must be stored flat; the optical fibres must not be folded or crushed.
Avoid exposure to very dusty environments. Avoid storage and use of flammable materials such as oxygen and
some anaesthetics in the treatment room.
The intermediate unit may be held on the main unit using the dedicated housing.
3.7.
Inspection of the system
After unpacking the FLUXMEDICARE® V2 device, inspect it and check it has not suffered any damage
during transport.
Before use, make sure the device has not been damaged, that the various parts are intact, e.g.
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The various parts are not broken
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The sheath connecting the main unit of the Medical Device and the intermediate unit should not be
damaged in any way (particularly cuts, even partial, pinching). The devices for connecting the sheath to
the unit must not be loose.
•
The seams on the cap are in good condition
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The textile optical fibres are not damaged
If damage is observed, contact MDB TEXINOV® before use.
3.8.
Preparation of the source before treatment
Environment
The equipment must be used by health professionals practising in doctors’ surgeries, hospitals and
clinics. Do not use in conditions where the ambient temperature exceeds 30°C or where there is
condensation.
Installation
The FLUXMEDICARE® V2 source from MDB TEXINOV® must be installed on a stable flat surface. Particular
attention should be paid to checking that the ventilation outlets are not obstructed (see §2.1). Sufficient
space between the front and rear panels and the adjacent surface must be maintained, in order to prevent any
obstruction of the air flows that could cause internal overheating of the system.
The protective intermediate unit cap must be removed before the textile is connected.