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Using FLOVAC® disposable collection system:
Before connecting the disposable collection system, remove the white ring fitted on the tank holder for
a more comfortable insertion of the same container.
Connect the short tube with the throttle connector marked as “VACUUM” fitted on the lid of the disposable pocket. The container should be positioned on
ON. The long silicon tube should be connected with the connector marked as “PATIENT”.
In order to perform suction, close the connector marked as “TANDEM” with the lid provided.
If using the equipment with FLOVAC® disposable collection system antibacterial filters are not required since each disposable pocket is already provided
with an inside filter. The hydrophobic antireflux and antibacterial filter provided will protect the equipment, while also acting as float valve deactivating
vacuum generation when the maximum volume level is reached.
When the float valve intervenes signalling the device is too full, the suction source must be disconnected within no more than 5 minutes.
Warning: The accidental inversion of connections may cause contamination for the operator and/or for the vacuum generation equipment.
NEVER USE THE DEVICE WITHOUT JAR AND / OR PROTECTION FILTER
MAKE SURE THAT CHILDREN AND/OR MENTALLY ILL PEOPLE DO NOT USE THE DEVICE WITHOUT ADULT SURVEILLANCE
ALWAYS PLACE THE DEVICE IN POSITIONS FOR EASY DISCONNECTION.
RULES FOR RETURNING AND REPAIRING
COMPLYING WITH THE NEW EUROPEAN RULES, GIMA INDICATES THE IMPORTANT POINTS TO PROTECT INSTRUMENT AND
OPERATORS HYGIENE.
THESE RULES MUST BE RESPECTED IN ORDER TO GUARANTEE HYGIENE AND SAFETY TO ALL THE PEOPLE OPERATING WITH THE
INSTRUMENT TO OBTAIN QUALITY AND WELL BEING.
GIMA warrants it’s products for
24 months
after purchasing date.
In front of this warranty, GIMA S.p.A. will be obliged only to repair or substitute free of charge the products or parts of them that, after verification effected on
our factory, or our authorized Service Center, by the Technical Service, results defective.
The product must be accompanied by a description of the defect.
The warranty, with exclusion of responsibility for direct and indirect damages, it is thought limited to the solos defects of material or workmanship and it
stops having effect when the device results however gotten off, tampered or sheltered out of the Factory or from the Authorized Service center.
The commodity always travels to risk and danger of the buyer, without any responsibility of GIMA for damages caused by the transport or dismay from the
vector.Every returned instrument will be hygienically checked before repairing.
If GIMA finds instrument not suitable for repairing due to clear signs of internal or external contamination, the same will be returned to customer with
specification of NOT REPAIRED INSTRUMENT, accompanied by an explanation letter.
GIMA will decide if contamination is due to bad functioning or misuse. If contamination is due to bad functioning, GIMA will substitute the instrument, only if
a SALE RECEIPT and STAMPED GUARANTEE accompany the same.
GIMA is not responsible for contaminated accessories, they will be substitute at customer's expenses.
For this reason it is
COMPULSORY
to carefully disinfect the external part of the instrument and accessories with a cloth soaked in methylated spirits or
hypochlorite-based solutions. Put the instrument and accessories in a bag with indication of disinfecting. We also request to specify the kind of fault, in order
to speed up repairing procedures.
To this end, please read the instructions carefully in order to avoid damaging the equipment through improper use.
Always specify the fault encountered so that GIMA can establish whether it falls into the category of the faults covered by the guarantee.
The manufacturer cannot be held liable for accidental or indirect damages should the device be modified, repaired without authorization or
should any of its component be damaged due to accident or misuse.
Any minimal modification / repair on the device voids the warranty and does not guarantee the compliance with the technical requirements
provided by the MDD 93/42/EEC Directive and its normatives.
