16
CLEANING DEVICE
Use a soft dry cloth with not-abrasive and not – solvent detergents.
BEFORE STRATING CLEANING OPERATIONS, MAKE SURE THAT INTERNAL PARTS OF DEVICE DON’T COME INTO
CONTACT WITH LIQUIDS AND THE AC/DC SWITCHING ADAPTER ARE DISCONNECTED.
This section contains information regarding the conformity of the compliance with the IEC 60601-1-2 Standard.
The SUPER VEGA BATTERYsurgical 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.
Mobile and portable RF communication appliances (mobile phones, transceivers, etc..) can affect the medical system.
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.
Guidance and manufacturer’s declaration – Electromagnetic Emissions
The surgical aspirator SUPER VEGA BATTERYis intended for use in the electromagnetic environment specified below. The customers or the
user of the surgical aspirator SUPER VEGA BATTERYshould assure that it’s used in such an environment.
Emissions Test
Compliance
Electromagnetic environment - guidance
Irradiated / Conducted emissions CISPR11
Group 1
The surgical aspirator SUPER VEGA BATTERYonly 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
appliances.
Irradiated / Conducted emissions CISPR11
Class [B]
The surgical aspirator SUPER VEGA BATTERYcan be used in all
environments, including domestic and those connected directly to the
public mains distribution that supplies power to environments used for
domestic scopes or environments feeds to you from batteries.
Harmonic emissions IEC/EN 61000-3-2
Class [A]
Voltage fluctuations / flicker emissions
IEC/EN 61000-3-3
Complies
Guidance and manufacturer’s declaration – Immunity Emissions
The surgical aspirator SUPER VEGA BATTERYis intended for use in the electromagnetic environment specified below.
The customers or the user of the surgical aspirator SUPER VEGA BATTERYshould assure that it’s used in such an environment.
Immunity Test
Level indicated by the
IEC 60601-1-2
Compliance Level
Electromagnetic environments - guidance
Electrostatic discharge
(ESD)
IEC/EN 61000-4-2
± 6kV on contact
± 8kV in air
The device doesn’t
change its state
Floors should be wood, conceret or ceramic
tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical fast transient
/ burst
IEC/EN 61000-4-4
± 2kV power supply lines
± 1kV for input / output lines
The device doesn’t
change its state
Mains power quality should be that of a typical
commercial environment or hospital or
environments feeds to you from batteries.
Surge
IEC/EN 61000-4-5
± 1kV differential mode
The device doesn’t
change its state
Mains power quality should be that of a typical
commercial environment or hospital or
environments feeds to you from batteries.
Loss of voltage, brief
voltage interruptions
and variations
IEC/EN 61000-4-11
5%U
T
(>95% dip U
T
) for 0.5 cycle
40%U
T
(>60% dip U
T
) for 5 cycle
70%U
T
(>30% dip U
T
) for 25 cycle
<5%U
T
(>95% dip U
T
) for 5 sec
-
Mains power quality should be that of a typical
commercial environment or hospital If the user
of the surgical aspirator SUPER VEGA
BATTERYrequest that the appliance operates
continuosly, the use of a continuity unit is
recommended.
Magnetic field
IEC/EN 61000-4-8
3A/m
The device doesn’t
change its state
The power frequency magnetic field should be
measured in the intended installation location
to assure that it’s sufficiently low.
Note U
T
is the value of the power supply voltage
