Gima SUPERVEGA EVO Bedienungsanleitung Seite 27

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• Check the operation of the bracket (without suction unit) by repeatedly acting on the seal hook. The move-
ment must be free from obstructions.
• Always make sure that the fixing screws are tightened correctly;
• Fit the suction unit in the bracket as indicated in Chapter "Securing the SUPERVEGA EVO suction device";
• Visually check (as per TAB II) the activation of the LCD screen.
In the event one or more phases fail, refer to the technical service.
Do not tamper with mechanical and/or electrical parts as this may affect the safety and efficiency of the
device.
No electrical and/or mechanical part of the support bracket has been designed to be repaired by the manu-
facturer, customer, and/or user. Always refer to the authorised technical service.
Maintenance and reuse
Once the device has been fitted in the bracket, always make sure that, upon activation, the LCD screen con-
firms the charge in progress of the internal battery (rif. TAB.I and TAB.II).
When using emergency vehicles, always check the housing of the suction unit in the support bracket at the
end of the intervention.
In case of accidents or collisions of the emergency vehicle, always request the authorised technical service
to check the support bracket and the suction unit.
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 EVO SUCTION UNIT surgical aspirator is an electro-medical device that requires particu-
lar precautions regarding electro-magnetic compatibility and which must be installed and commissioned ac-
cording 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 mal-
functions). The use of accessories, transducers and cables differing from 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.
Guidance and manufacturer's declaration – electromagnetic Emissions
The SUPERVEGA EVO SUCTION UNIT is intended for use in the electromagnetic environment specified below. The
customers or the user of the SUPERVEGA EVO SUCTION UNIT should make sure that it's used in such an environment.
Emissions test
Irradiated / Conducted
emissions CISPR11
Irradiated / Conducted
emissions CISPR11
Harmonic emissions
EN 61000-3-2
Voltage fluctuations / flicker
emissions EN 61000-3-3
Compliance Electromagnetic environment - guidance
Group 1 The SUPERVEGA EVO SUCTION UNIT only used RF energy only
for its internal functioning. Therefore, its RF emissions are very low
and are not cause interference in proximity of any Electronic appli-
ances.
Class [B] The SUPERVEGA EVO SUCTION UNIT can be used in all environ-
ments, including domestic and those connected directly to the public
mains distribution that supplies power to environments used for do-
Class [A]
mestic scopes.
Complies
ENGLISH