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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 WITH 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

•  Complete aspiration jar 1000ml

•  Conical fitting

•  Tubes set 6mm x 10mm (trasparent silicon)

•  Aspiration probe CH20

•  Antibacterial and hydrophobic filter

Available under request with different versions with complete jar 2000ml.

Anti-bacterial and hydrophobic filter: designed for the individual patient to protect patient and machine from 

cross-infections. Prevents the liquids, that come into contact with it, from passing through it. 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 known and/or there is no risk of indirect contamination, 

the filter should be replaced after every work shift or once a month even if the device is not used. 

Suction catheter: Single-use device to be used on a single patient. Do not wash or re-sterilize after use. 

Reuse may cause cross-infections. Don’t use after lapse of the sell-by date

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 to 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. 

Working Condition

Room temperature: 5 ÷ 35°C 

Room humidity percentage: 10 ÷ 93% RH 

Atmospheric pressure: 700 ÷ 1060 hPa

Conservation condition and Transport

Room temperature: -25 ÷ 70°C 

Room humidity percentage: 0 ÷ 93% RH 

Atmospheric pressure: 500 ÷ 1060 hPa

Summary of Contents for 28210

Page 1: ...HIRURGISCHER ABSAUGER VEGA ASPIRADOR QUIR RGICO VEGA APARELHO DE SUC O CIR RGICO VEGA M28210 M Rev 7 12 20 PROFESSIONAL MEDICAL PRODUCTS Gima S p A Via Marconi 1 20060 Gessate MI Italy gima gimaitaly...

Page 2: ...rtment Do not attempt to make the device work before it has been thorough ly checked by qualified personnel and or the GIMA technical service department Position the device on stable and flat surfaces...

Page 3: ...nce they contain small parts that may be swallowed 14 Do not leave the device unattended in places accessible to children and or persons not in full possession of mental facultiesas they may strangle...

Page 4: ...on 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...

Page 5: ...of local laws and regulations The jug and lid can be further disinfected using a common disinfectant strictly following the instructions and dilution values provided by the manufacturer At the end of...

Page 6: ...nents list descriptions setting in structions and any other information that can help the technical assistance staff for product repair BEFORE EVERY CHECKING OPERATION IN CASE OF ANOMALIES OR BAD FUNC...

Page 7: ...the presence of liquids or other visible contamination secretions In the presence of liquids or other visible contamination immediately replace the medical device due to the risk of an insufficient v...

Page 8: ...d cables sold by the appliance and system manufacturer as spare parts can lead to an increase in emissions or in a decrease of the immunity of the device or system The following tables supply informat...

Page 9: ...ains power quality should be that of a typi cal commercial environment or hospital If the user of the VEGA SUCTION UNIT request that the appliance operates continuously the use of a continuity unit is...

Page 10: ...es such as changing the device s direction or positioning may be necessary b The field intensity on an interval frequency of 150 kHz to 80 MHz should be less than 3 V m Recommended separation distance...

Page 11: ...EEE disposal Class II applied Serial number Temperature limit Fuse Atmospheric Pressure limit IP21 Covering Protection rate Alternating current ON Hz Mains frequency OFF Humidity limit SYMBOLS Disposa...

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