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If the overfill security system it’s activated, don’t proceede with the liquid aspiration. If the overfill security
system doesn’t work there are two cases:
1° case – If the overfill security system doesn’t work the aspiration will be stopped by the bacteriological filter
who avoid the liquid penetration inside the device.
2° case – If both the security system doesn’t work, there is the possibility that liquid comes inside the device,
in this case return the device to GIMA technical service.
GIMA S.p.A. will provide upon request electric diagrams, components list, descriptions, setting in-
structions and any other information that can help the technical assistance staff for product repair.
The medical device contains firmware. This information is made available in order to assist the tech-
nical assistance personnel in the eventual repair of the appliance.
BEFORE EVERY CHECKING OPERATION, IN CASE OF ANOMALIES OR BAD FUNCTIONING,
PLEASE CONTACT GIMA TECHNICAL SERVICE. GIMA DOES NOT GIVE GUARANTEE IF INSTRU-
MENT, AFTER THE TECHNICAL SERVICE CHECKING, APPEARS TO BE TAMPERED.
INSTRUCTION FOR USE
• The device must be checked before each use in order to detect malfunctions and / or damage caused by
transport and / or storage.
• The working position must be such as to allow one to reach the control panel and to have a good view of
the LCD screen, the suction tank and the antibacterial filter.
WARNING: For proper use, place the aspirator on a flat, stable surface in order to have the full volume
of use of the jar and better efficiency of the overflow device.
Operation with Internal Battery
• Connect the short silicon tube, with antibacterial filter, to the suction connector (VACUUM). The other tube,
with one end connected to the antibacterial filter with the other end to jar’s lid connector where has been
fixed the red float. When the 90% of the volume of the jar is reached there is the activation of the security
float (the float close the aspiration connector on the jar) to the avoid liquid penetration inside the device.
Filter assembling
Make sure the filter is assembled with the arrows on the side of the patient.
WARNING: The inside of the medical device must be regularly checked for the presence of liquids or other
visible contamination (secretions). In the presence of liquids or other visible contamination, immediately re-
place the medical device due to the risk of an insufficient vacuum flow rate.
These products have been designed, tested and manufactured exclusively for single patient use and for a
period no longer than 24 hours.
• Connect the long silicon tube to the other jar’s lid connector (PATIENT PORT);
• To start the treatment press the ON/OFF button and check its green back-light. When the device is switched
on the LCD screen activates displaying a bar-graph, graduated scale, and negative pressure value, which
must be set by the operator;
ENGLISH
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