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

PERIODICAL MAINTENANCE CHECKS

The SUPERVEGA EVO suction equipment does not need maintenance or lubrication.

It is, however 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. Remove 

the appliance from the box and always check that the plastic parts and AC/DC adaptor are intact which may 

have been damaged during previous use. Connect the universal transformer to the device using the relevant 

connector and insert the power cable plug of the adaptor in the power socket. After starting the device, block 

off the suction nozzles with your finger and check for suction.

Make sure you do not hear excessively annoying noises that may highlight a malfunction.

The device is protected by a protective fuse (F 10A L 250V) located in the cigarette lighter cable. Always 

check the type and amperage indicated when replacing it.

 

Internally, the device (see electrical sheet) is pro-

tected by two fuses F1 and F2 (F 15A L 125V), which cannot be reached from the outside; refer to technical 

personnel authorised by the manufacturer to replace them.

The device is equipped with a Lithium-Ion Battery, which cannot be reached from the outside. Only refer to 

GIMA technical service personnel to replace it.

 Only use batteries recommended by Gima. Use of batteries other than those recommended 

will make the warranty void and null.

Only qualified personnel are authorised to replace the internal battery. Any operation Performed by 

non-trained personnel may cause danger (e.g. Excessive temperature)

The device should be checked at least once every 12 months by technical service. Every 24 months it is 

compulsory to have a safety inspection and technical maintenance performed on the device.

ENGLISH

Typical defect

Cause

Remedy

1. Steady Red Back-Light

Low battery

If equipped with an AC/DC power supply, con-

nect  the  power  cable  to  the  mains,  with  the 

switch not pressed and leave it to charge until 

a Steady White Back-Light is shown (ref. TAB.I)

2. No Led On and Back-Light 

failure

Device locked

Internal  technical  problem.  Contact  technical 

assistance.

3. No aspiration

Vessel lid screwed incorrectly

Unscrew and tighten the lid of the vessel

4. No aspiration

Cover gasket not in place

Unscrew the cover and reposition the gasket in 

its cover housing.

5. Blocked float

Fouling on the float

Unscrew  the  cover,  remove  the  float  and  pro-

ceed with cleaning.

6. Failure to close the float

If the cap has been washed, check that 

the float is not partially detached

Wedge float

7. Slow aspiration

Foam  formation  inside  the  collecting 

vessel

Fill the vessel 1/3 full of normal water

8. No aspiration caused by 

mucus leakage

Clogged filter

Replace the filter

9. Low and/or no vacuum 

power

•  Unsuitable aspiration level

•  Protection filter blocked

•  Connection pipes to the filter and the 

device  blocked,  kinked  or  discon-

nected

•  Overflow valve closed or blocked

•  Damaged pump

•  Proceed to set the correct aspiration value

•  Filter replacement

•  Connect the pipes to the filter and/or vessel or 

replace them if clogged

•  Unblock  the  overflow  valve,  hold  the  device 

upright

•  Contact the Gima technical service

Defects 1 - 2 - 3 - 4 - 5 - 6 - 

7 - 8 - 9 

None of the remedies was effective

Contact your Gima dealer or service centre

Summary of Contents for 28183

Page 1: ...ASPIRATEUR SUPERVEGA EVO ABSAUGER SUPERVEGA EVO ASPIRADOR SUPERVEGA EVO M28183 M Rev 1 01 21 PROFESSIONAL MEDICAL PRODUCTS Gima S p A Via Marconi 1 20060 Gessate MI Italy gima gimaitaly com export gimaitaly com www gimaitaly com Made in Italy 28183 0476 ...

Page 2: ...ontact Gima technical service 2 Before connecting the device always check that the electrical details indicated on the data label and the type of plug used correspond to those of the electrical network to which you intend to connect it 3 Comply with the safety rules indicated for electrical equipment and in particular Use only original accessories and components supplied by the manufacturer Gima i...

Page 3: ... product and its parts are biocompatible in accordance with the requirements of the EN 60601 1 standard 11 The operation of the device is very simple and therefore no further measures are required other than those indicated in the following user manual 12 The lithium ion battery contained within the medical device should not be considered normal household waste Dispose of this component at a suita...

Page 4: ...Replace it when ever you suspect that it may be contaminated and or it becomes wet or discoloured Replace the filter every time it is used if the suction pump is used on patients in unknown pathological situations and where an assess ment of indirect contamination is not possible The filter is not manufactured to be decontaminated dismantled and or sterilised If however the patient s pathology is ...

Page 5: ...ure not exceeding 60 C Once again carefully wash each single part using if necessary a non abrasive brush to remove any de posits 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 manu facturer After cleaning leave the parts to dry in an open ...

Page 6: ...nal battery Any operation Performed by non trained personnel may cause danger e g Excessive temperature The device should be checked at least once every 12 months by technical service Every 24 months it is compulsory to have a safety inspection and technical maintenance performed on the device ENGLISH Typical defect Cause Remedy 1 Steady Red Back Light Low battery If equipped with an AC DC power s...

Page 7: ...creen 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 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 li...

Page 8: ...ment of separation from the electrical mains even if the device is equipped with an on off button Once the device is in use the power plug must remain accessible to allow another method of disconnection from the electrical mains The device features an energy saving function which allows the device to increase its autonomy and de crease the number of revs of the motor In order to do so it controls ...

Page 9: ...t and fixed activation of the bargraph During the Charge phase Charging cycle complete Remove the device from the support plate of the ambulance Fixed green back light During battery operation Primary status Battery fully charged Battery operation guaranteed Fixed yellow back light During battery operation Intermediate status Battery not fully charged Battery operation guaranteed start the charge ...

Page 10: ...the Function off the device is activated deactivated by pressing the ON OFF key RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REMEDIES This section contains information regarding the conformity of the compliance with the EN 60601 1 2 Standard 2015 The SUPERVEGA EVO SUCTION UNIT surgical aspirator is an electro medical device that requires particu lar precautions regarding electro magnetic comp...

Page 11: ...nt Immunity Test Level indicated by the EN 60601 1 2 Compliance Level Electromagnetic environment guidance Electrostatic discharge ESD EN 61000 4 2 8kV on contact 15kV in air The device doesn t change its state Floors should be wood concrete or ceramic tile If floors are covered with synthetic ma terial the relative humidity should be at least 30 Electrical fast transient burst EN 61000 4 4 2kV po...

Page 12: ...etermined by an elec tro magnetic study of the sitea could be lower than the level of conformity of each frequency interval b It is possible to check for interference in proximity to devices identified by the fol lowing symbol Note 1 At 80 MHz and 800 MHz the interval with the highest frequency is applied Note 2 These guide lines may not be applicable in all situations The electro magnetic propaga...

Page 13: ... 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 the transmitter frequency where P is the maximum nominal output power of the transmitter in Watt W depending on the transmitter s manufacturer Note 1 At 80 MHz and 800 MHz the interval with the highest frequency is applied No...

Page 14: ...ed of correctly you will help prevent potentially negative consequences for the environment and human health which could otherwise be caused by inappropriate waste handling of the battery The recycling of the materials will help to conserve natural resources At the end of their life hand the batteries over to the applicable collection points for the recycling of waste batteries For more detailed i...

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