Gima SUPERVEGA BATTERY Bedienungsanleitung Seite 22

NEVER USE THE DEVICE WITHOUT JAR AND / OR PROTECTION FILTER
Using FLOVAC® disposable collection system:
Before connecting the disposable collection system, remove the blu ring fitted on the tank holder for a more
comfortable insertion of the same container.
• After opening the package, fully stretch the bag and then flatten it concentrically to eliminate as much air
as possible.
• Insert the bag and apply the cover to an appropriately sized reusable rigid container by pressing firmly
around the entire perimeter. Make sure that the system is completely sealed.
• Close the connector marked as "TANDEM" with the lid provided.
• Connect the power source of the vacuum to the VACUUM port equipped with specific reusable conical
fitting with "male" connection.
• Connect the patient tube to the PATIENT port of the cover
• Before use, check all closures and make sure there are no leaks, starting the aspiration source. If the bag
expands to fully adhereto the walls of the rigid container and the cover bends towards the inside of the
glass, the system is not leaking.
• Start the aspiration and periodically check the filling level of the container. The overflow valve will cause the
interruption of aspiration if the aspirated fluids have reached the maximum filling level of the device.
• When the 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 contains information regarding the conformity of the compliance with the EN 60601-1-2 Standard
(2015).
The SUPERVEGA BATTERY SUCTION UNIT surgical aspirator is an electro-medical device that requires
particular precautions regarding electro-magnetic compatibility and which must be installed and commis-
sioned according to the electro-magnetic compatibility information supplied. Portable and mobile radio com-
munication devices (mobile phones, transceivers, etc.) may interfere with the medical device and should not
be used in close proximity with, adjacent to or on top of the medical device. If such use is necessary and
unavoidable, special precautions should be taken so that the electro-medical device functions properly in its
intended operating configuration (for example, constantly and visually checking for the absence of anomalies
or malfunctions). The use of accessories, transducers and cables differing from those specified, with the ex-
ception of transducers and 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
information regarding the EMC (Electromagnetic Compatibility) characteristics of the electro-medical device.
ENGLISH
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