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17

eNgLIsh

• Disconnect all tubes from the jar and the protection filter

• Wash each part of the container from secretions under cold running water and then clean every

single part in hot water (temperature not exceeding 60°C)

• Once again, carefully wash each single part using, if necessary, a non-abrasive brush to remove

any deposits. Rinse with hot running water and dry all parts with a soft cloth (non-abrasive). It is

possible to wash with commercial disinfectants by carefully following the instructions and dilution

values supplied by the manufacturer. After cleaning, leave the parts to dry in an open, clean envi-

ronment.

• Dispose of the aspiration catheter according to that provided by local laws and regulations.

The silicone aspiration tubes and the conical fitting may be carefully washed in hot water (temperature 

must not exceed 60°C). After cleaning, leave the parts to dry in an open, clean environment.
When cleaning is complete, reassemble the container for liquid aspirations according to the following 

procedure:

• Place the overflow valve into its seat in the cover (under VACUUM connector)

• Insert floating valve keeping the o-ring towards the opening of the cage

• Place the o-ring into its seat around the cover

• After completing assembling operations always make sue that cover seals perfectly to avoid vacu-

um leackages or liquid exit

After disposing of disposable parts and disassembling the jar wash in running cold water and rinse 

thouroughly. Then soak in warm water (temperature shall not exceed 60°C). Wash thouroughly and if 

necessary use a non-abrasive brush to remove incrustations. Rinse in running warm water and dry all 

parts with a soft cloth (non-abrasive). The jar and the cover can be autoclaved by placing the parts into 

the autoclave and running one sterilization stem cycle at 121°C (1 bar relative pressure – 15 min) ma-

king sure that the jar is positioned upsidedown. Mechanical resistance of the jar is guaranteed up to 30 

cycles of sterilization and cleaning at the indicated conditions (EN ISO 10079-1). Beyond this limit the 

physical-mechanical characteristics of the plastic may decrease and replacement of the part is therefore 

recommended. After sterilization and cooling at environment temperature of the parts make sure that 

these are not damaged. The aspiration tubes can be sterilized on autoclave using a sterilization cycle 

at 121°C (1 bar relative pressure – 15 min). The conical connector can be sterilized on autoclave using 

a sterilization cycle at 121°C (1 bar relative pressure – 15 min).

 DO NOT WASH, STERILIZE OR PUT IN AUTOCLAVE THE ANTIBACTERIAL FILTER 

Instruction for disposal Liner Flovac®: 

If the device is equipped with disposable collection systems FLOVAC ® carry out the disposal of the bag 

as follows: turn off the Vacuum and remove all the tubes connected to the Liner, giving particular atten-

tion to avoid accidental contamination. Fit the appropriate plugs to the “PATIENT” and “TANDEM” ports, 

pressing the home firmly, taking care to avoid accidental contamination. Turn the butterfly connector to 

OFF. Remove the liner bag from the rigid container and transfer it to the waste disposal area, ensuring 

that all the openings are sealed, keeping in mind the product is potentially infectious. This product must 

be disposed of in accordance with the current hospital regulations.

PERIODICAL MAINETANCE CHECKS

The TOBI HOSPITAL suction equipment does not need maintenance or lubrication. It is, however, ne-

cessary to inspect the unit before each use. With regard to training, given the information contained in 

the user manual and since it is easy to understand the said device, it doesn’t appear to be necessary. 

The device must be checked before each use in order to detect malfunctions and / or damage caused 

by transport and / or storage.

Always check the integrity of the footswitch power cord. Connect cable to electrical network and turn 

switch on. Close the aspiration outlet with your finger and with suction regulator in maximum vacuum 

position check that the vacuum indicators reaches -90 kPa (-0.90 bar) maximum. Rotate the knob from 

right to left and check the aspiration regulating control. The vacuum indicator should go down -40 kPa 

(-0.40 bar). Verify that loud noises are not present, these can indicate wrong functioning. A protection 

fuses 

(F 1 x 1.6 A L 250V)

 reachable from exterior and situated in the plug protects the instrument. For 

fuses replacing, always the type and the range. Before changing the fuse, disconnect the plug from the 

power supply socket. Internally, the device (only for devices fitted with a circuit board) is protected by a 

Summary of Contents for TOBI HOSPITAL

Page 1: ...ASPIRATEUR TOBI HOSPITAL CHIRURGISCHER ABSAUGER TOBI HOSPITAL ASPIRADOR QUIR RGICO TOBI HOSPITAL 28202 28232 28233 28234 M28202 M Rev 7 01 21 Gima S p A Via Marconi 1 20060 Gessate MI Italy gima gima...

Page 2: ...unstable surfaces which may cause it to acci dentally fall and lead to a malfunction and or breakage Should there be signs of damage to the plastic parts which may expose inner parts of the energised...

Page 3: ...ive and its normatives Under certain failure conditions the temperature of the casing may become hot and there may be a risk of burns if you touch those parts In any case the temperatures do not excee...

Page 4: ...anteed up to 30 cycles of cleaning and sterilization Beyond this limit the physical chemical characteristics of the plastic material may show signs of decay Therefore we recommend that you to change i...

Page 5: ...nd cooling at environment temperature of the parts make sure that these are not damaged The aspiration tubes can be sterilized on autoclave using a sterilization cycle at 121 C 1 bar relative pressure...

Page 6: ...After sales Assistance Service 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...

Page 7: ...e jar is reached there is the activation of the security float the float close the aspiration connector on the jar to avoid liquid penetration inside the device The device must be used on a plan of ho...

Page 8: ...cover bends towards the inside of the glass the system is not leaking Start the aspiration and periodically check the filling level of the container The overflow valve will cause the interruption of a...

Page 9: ...it s used in such an environment Immunity Test Level indicated by the EN 60601 1 2 Compliance Level Electromagnetic environments guidance Electrostatic discharge ESD EN 61000 4 2 8kV on contact 15kV i...

Page 10: ...fixed RF transmitters as determined by an electromagnetic site study of the site should be less that the com pliance level in each frequency range Interference may occur in the vicinity of equipment...

Page 11: ...3 10 3 8 3 8 7 3 100 12 12 23 For transmitters with a maximum nominal output power not shown above the recommended separation distance in metres m can be calculated using the equation applicable to t...

Page 12: ...specifications may change without notice Disposal The product must not be disposed of along with other domestic waste The users must dis pose of this equipment by bringing it to a specific recycling p...

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