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18

INSTRUCTION FOR USE

•  The device must be checked before each use in order to detect malfunctions and / or damage caused by 

transport and / or storage.

•  The working position must be such as to allow one to reach the control panel and to have a good view of 

the empty indicator, the jar and the antibacterial filter.

•  It is recommended not to keep the device in your hands and / or to avoid prolonged contact with the body 

of apparatus.

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.

•  Connect one end of the short silicon tube, with antibacterial filter, to the suction connector on the lid of the 

jar.

•  The other tube, connected to the filter on one end, must be attached to the connector on the flask cover to 

which the float is secured inside. (overflow device). The overflow device starts working (the float closes the 

connector on the cover) when the maximum volume of liquid is reached, so no liquid can enter the machine 

(90% of the flask’s total volume), thus ensuring that the liquid cannot penetrate inside the machine. The 

device must be used on a flat work top. 

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 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 vacuum flow rate.

These products have been designed, tested and manufactured exclusively for single patient use and 

for a period no longer than 24 hours.

•  Connect the long silicone tube to the “PATIENT” jar outlet

•  Connect the other end of the long silicon tube to the probe plastic connector, then connect the suction 

probe to it.

•  Connect the power cord to the device then connect the plug to the electrical mains supply.

•  Push switch on position I to start suction.

•  Unscrew the lid of the jar and fill the jar 1/3 full or ordinary water (this assists the unit to reach peak vacuum 

performance and makes clean-up easier) then re-screw the lid on the jar correctly.

•  During operation the jar has to be in vertical position to avoid overflow valve to cut off aspiration. Should 

this happen, switch off the device and disconnect the tube from the jar cover (from “VACUUM” outlet).

•  Once finished push switch on O position and unplug.

•  Remove the accessories and clean.

•  At the end of each use, place the device in its box away from dust.

WARNING: The power supply cable plug is the element of separation from the electrical mains system: even 

if the units equipped with a special on / off switch button, the power supply plug must be kept accessible once 

the device is in use so as to allow a further method of disconnection from the mains supply system.

ENGLISH

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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