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eNgLIsh

TOBI HOSPITAL is a surgical aspirator power-fed at 230V ~ / 50Hz, to be used for suctioning body liquids 

(such as mucus, phlegm and blood) provided with 4 antistatic wheels, two of which with braking device, 

and a pulling handle.

This equipment is designed for easy transport and continuous utilization.

Thanks to these characteristics and to its functions, this device is particularly suitable for utilization in 

hospital wards and operation theatres both for suctioning body liquids and for gynaecological and der-

matological (liposuction) applications.

It’s provided with a plastic body, with thermal and electrical isolation in compliance with European safety 

standards, two complete suction tanks in polycarbonate suitable for sterilization, and a float valve, besi-

des being fitted with a suction regulator and a vacuum gauge on the front panel. Available under request 

with differents versions for applications and use (version with remote control, version with 4 litre jars, 

version with flow direction regulator).

Read instruction manual carefully before use

Only highly qualified staff use reserved

The instrument must not be disassembled. for a technical service always contact GIMA

IMPORTANT SAFETY RULES:

1. Check the condition of the unit before each use. The surface of the unit should carefully inspected for

visual damage. Check the mains cable and do not connect to power if damage is apparent;

2. Before connecting the appliance always check that the electric data indicated on the data label and

the type of plug used, correspond to those of the mains electricity to witch it’s to be connected;

3. Respect the safety regulations indicated for electrical appliances and particularly:

• Use original components and accessories provided by the manufacturer to guarantee the highest

efficiency and safety of the device;

• The device can be used only with the bacteriological filter;

• Never immerge the appliance into water;

• Position the device on stable and flat surfaces in a way that the air inlets on the back aren’t obstructed;

• To avoid incidents, do not place the aspirator on 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 device, do not connect the plug to the

electrical socket. Do not attempt to make the device work before it has been thoroughly checked by

qualified personnel and/or the GIMA technical service department.

• Don’t use in the presence of inflammable substances such as anaesthetic, oxygen or nitrous oxide;

• Don’t touch the device with wet hands and always prevent the appliance coming into contact with

liquids;

• Don’t leave the appliance connected to the power supply socket when not in use;

• Don’t pull the power supply cable to disconnect the plug remove the plug from the mains socket

correctly;

• Store and use the device in places protected against the weather and far from any sources of heat.

After each use, it is recommended to store the device in its own box away from dust and sunlight.

• In general, it is inadvisable to use single or multiple adapters and/or extensions. Should their use be

necessary, you must use ones that are in compliance with safety regulations, however, taking care not

to exceed the maximum power supply tolerated, which is indicated on the adapters and extensions.

4. For repairs, exclusively contact technical service and request the use of original spare parts. Failure

to comply with the above can jeopardise the safety of the device;

5.

Use only for the purpose intended.

 Don’t use for anything other than the use defined by the manu-

facturer. The manufacturer will not be responsible for damage due to improper use or connection to

an electrical system not complying with current regulation.

6. Instrument and accessory discharging must be done according to current regulations in the country

of use.

7.

WARNING:

 Do not change this equipment without the permission of the manufacturer. None of elec-

tric or mechanical parts have been designed to be repaired by customers or end-users. Don’t open

the device, do not mishandle the electric / mechanical parts. Always contact technical assistance

8. Using the device in environmental conditions different than those indicated in this manual may harm

seriously the safety and the technical characteristics of the same;

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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