Risk Of Electromagnetic Interference And Possible Rem- Edies - Gima 28200 Manual Del Usuario

Press the button marked as (---) to perform suction using the footswitch control and execute intermittence
work cycles. Press the button marked as (-) to perform remote suction using the footswitch control (continuous
suction). To stop suction just push on the footswitch control with strength. Press the ON/OFF button to stop
the medical equipment. Before removing the feeding plug, ensure autotest has been performed on the panel.
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 adhere to 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 5 minutes.
RISK OF ELECTROMAGNETIC INTERFERENCE AND POSSIBLE REM-
EDIES
This section contains information regarding the conformity of the compliance with the EN 60601-1-2 (2015)
Standard.
CISPR group and category classification: group 1, category B.
The HOSPI PLUS surgical aspirator is an electro-medical device that requires particular precautions regarding
electro-magnetic compatibility and which must be installed and commissioned according to the electro-
magnetic compatibility information supplied. Portable and mobile radio communication 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 different to those specified, with the exception 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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