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Charging operations (through the supplied AC/DC adapter): To charge the internal battery, connect the 

universal adaptor (supplied) to the mains electricity supply for about 6 hours (360 minutes) with the device 

switched off (not operating).

The symbol 

 positioned near the 12V jack on the casing requires the user to read the instructions before 

each use, identifying the model and type of power supply which can be connected through the information 

provided in the instructions for use.

LIGHT INDICATORS

The device is provided with a light indicator (directly on the LCD screen) which allows you to view the opera-

tion of the device, autonomy of the battery, and the charge phase in progress.

The light indications, which appear during operation, are indicated in table I.

The charge cycle starts automatically by placing the device on the specific support bracket (ref. Support 

Bracket and Charge Chapter). The charge occurs only when the motor of the suction unit is off.

DISPLAY IN CHARGE: this is on with white back-light and it remains on for the entire time. It switches off if 

there is no external voltage. The charge phase lasts until the device is powered and the battery is kept at its 

maximum charge. The large digits display “CHA” .

TAB. I – INDICATOR LIGHTS DURING OPERATIONS

TAB. II – WRITTEN SIGNALS / BUTTON LED SIGNAL

Back-light signals

Phase

Problem / Cause

Solution

Fixed white back-light 

and progressive activa-

tion of the bar-graph

During the Charge

phase

Battery charge in 

progress

Wait

Fixed white back-light 

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 

cycle upon activation of the red back-light

Fixed red back-light

During battery 

operation

Low battery

Start charge phase

ATTENTION: A long and continuous beep is 

produced during this signal to warn the opera-

tor about the low charge level of the battery.

Flashing red back-light Automatic switch-off 

of the device due to 

discharged battery

Battery fully discharged The flashing back-light switches on upon 

reactivation of the device. Immediately start 

the battery charge cycle.

ENGLISH

Button LED signal / 

written signal

Function

Colour

Position

ON/OFF button

Power on 

Green

Near the front panel key

Proximity Button

Switch the ON/OFF key

Blue

LED located above 

the “Proximity” key

CHA

Displays the battery 

charge status

Fixed white back-light and progres-

sive activation of the bargraph

Central in digits of large 

dimensions

Small three-digit 

number (000)

Displays the voltage of the 

device if in charge phase 

or it displays the full scale 

of the bar-graph.

Fixed white or green back-light 

depending on whether external 

power supply or battery and 

progressive activation of the 

bar-graph are used.

Sideways in small digits

Bar-graph 

(arc bar-graph)

It displays the trend of the 

negative pressure or of the 

charge status

Progressive activation of the 

bar-graph (black)

Arc-shaped in the middle 

of the screen

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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