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ENGLISH

The technical specifications may change without notice.

CLEANING OF THE DEVICE

Use a soft dry cloth with not – abrasive and not – solvent detergents. To clean the device external parts always 

use a cotton cloth dampened with detergent. Don’t use abrasive or solvent detergents. Before carrying out 

any cleaning and / or maintenance operation, disconnect the appliance from the power supply, unplugging it 

or turning off the switch on the device.

 Particular care should be taken to ensure that the internal parts of the equipment do not get in 

touch with liquids. Never clean the equipment under water.

During all clearing operations use protection gloves and apron (if need be, also wear a face mask and glass-

es) to avoid getting in contact with contaminating substances (after each utilization cycle of the machine).

ACCESSORIES SUPPLIES

•  N°2 complete aspiration jar 2000ml

•  Conical fitting

•  Tubes set 8 mm x 14 mm

•  Hydrophobic and antibacterial filter

•  AC/DC adapter

•  European power supply cord for AC/DC adapter

The filter is produced with (PTFE) hydrophobic material to prevent fluids entering the pneumatic circuit. 

It should be changed immediately if it becomes wet or if there is any sign of contamination or discolouration. 

If should also be changed if the unit is used with a patient whose risk of contamination is unknown. Don’t use 

the suction unit without the protection filter. If the suction unit is used in an emergency or in a patient where 

the risk of contamination is not known the filter must be changed after each use. 

The filter is not designed to be decontaminated, disassembled and/or sterilised. If the patient’s pathology is 

known and/or no risk of indirect contamination exists, it is advisable to replace the filter after each work shift 

or at any rate on a monthly basis even if the device is not used.

WARNING: Suction tubes for insertion in the human body purchased separately from the machine 

should comply with ISO 10993-1 standards on material biocompatibility. 

Aspiration jar: the mechanical resistance of the component is guaranteed 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 change it. 

Silicone tubes: the number of cycles of sterilization and/or cleaning is strictly linked to the employment of the 

said tube. Therefore, after each cleaning cycle, it is up to the final user to verify whether the tube is suitable 

for reuse. The component must be replaced if there are visible signs of decay of the material constituting the 

said component. 

Conical fitting: the number of cycles of sterilization and the number of cleaning cycles is strictly linked to 

the employment of the said component. Therefore, after each cleaning cycle, it is up to the final user to verify 

whether the fitting is suitable for reuse. The component must be replaced if there are visible signs of decay in 

the material constituting the said component. 

Working Condition

Room Temperature: 5 ÷ 35°C

Room Humidity Percentage: 30 ÷ 75% RH 

Atmospheric pressure: 800 ÷ 1060 hPa

Altitude: 0 ÷ 2000m s.l.m. 

Conservation condition and Transport

Room Temperature: - 40°C ÷ 70°C

Room Humidity Percentage: 10 ÷ 100% RH

Atmospheric pressure: 500 ÷ 1060 hPa

Summary of Contents for SUPERVEGA 28193

Page 1: ...EUR SUPERVEGA BATTERY SUR CHARIOT ABSAUGER SUPERVEGA BATTERY AUF TROLLEY ASPIRADOR SUPERVEGA BATTERY SOBRE CARRO M28193 M Rev 1 01 21 PROFESSIONAL MEDICAL PRODUCTS 0476 Gima S p A Via Marconi 1 20060...

Page 2: ...inlets on the back aren t obstructed To avoid incidents do not place the aspirator on unstable surfaces which may cause it to accidentally fall and lead to a malfunction and or breakage Should there...

Page 3: ...in chest fluids The device must not be used for suction of explosive corrosive or easily flammable liquids SUPERVEGA BATTERY SUCTION UNIT is not suitable for MRI Do not introduce the device in MRI env...

Page 4: ...use The filter is not designed to be decontaminated disassembled and or sterilised If the patient s pathology is known and or no risk of indirect contamination exists it is advisable to replace the f...

Page 5: ...rations 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 t...

Page 6: ...ttery pay special attention to the polarity of the same component The polarities are indicated directly on the battery If the overfill security system it s activated don t proceede with the liquid asp...

Page 7: ...se must be used in vertical mode to prevent the action of the backflow valve If this protection is triggered turn the device off and disconnect the pipe connected to the vacuum jar indicated with the...

Page 8: ...able to charge the internal battery it is necessary to connect the universal switching adapter to the electric network for approx 240 minutes with the main switch to position 0 TAB I INDICATOR LIGHTS...

Page 9: ...e float valve intervenes signalling the device is too full the suction source must be disconnected within no more than 5minutes RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REMEDIES This section...

Page 10: ...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...

Page 11: ...mined 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...

Page 12: ...2 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 frequenc...

Page 13: ...rectly 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...

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