Device Disposal; Electromagnetic Compatibility - FLAEM Aspira GO Manual De Instrucciones

SYMBOLS
Class II device
Type BF applied part
Attention: check the instruc-
tions for use
Single use
Alternating current
Ethylene oxide sterilisation
Expiry date
More vacuum
Direct current

DEVICE DISPOSAL

In compliance with the Directive 2012/19/EC, the symbol printed on the device shows that the device to be
disposed of is considered waste and must therefore be a "separate collection" item. Consequently, the user
must take it (or have it taken) to the differentiated collection sites provided by the local authorities, or turn it in
to the dealer when purchasing an equivalent new device. Differentiated waste collection and the subsequent
treatment, recycling and disposal procedures promote the production of devices made with recycled materials and
limit the negative effects on the environment and on health caused by potential improper waste management. The
unlawful disposal of the product by the user could result in administrative fines as provided by the laws transposing
Directive 2012/19/EC of the European member state or of the country in which the product is disposed of.

ELECTROMAGNETIC COMPATIBILITY

This device was designed to satisfy the current requirements for electromagnetic compatibility (EN 60 601-1-2).
Electro-medical devices require particular care during installation and use relative to EMC requirements. Users are
therefore requested to install and/or use these devices following the manufacturer's specifications. There is a risk of
potential electromagnetic interference with other devices, in particular with other analysis and treatment devices.
RF mobile or portable radio and telecommunications devices (mobile telephones or wireless connections) might
interfere with the operation of electro-medical devices. For further information visit our website www.flaemnuova.it.
The Medical Device may be subject to electromagnetic interference if other devices are used for specific diagnosis
or treatments.
Flaem reserves the right to make technical and functional modifications to the product with no prior warning.
Device serial number
TÜV approval
Minimum and maximum
room temperature
Minimum and maximum
atmospheric pressure
Minimum and maximum air moisture
Without latex
Protection rating of the
casing: IP21.
(Protected against solid
foreign objects larger than
IP21
12mm. Protected against ac-
cess with a finger; Protected
against vertically dripping
water).
Less vacuum
19
When
Switch on
switched off, the on/off
switch stops compres-
sor function in only one
phase of the two-phase
Switch off
power supply.
CE Marking medical ref. Dir 93/42 EEC
0051
and subsequent updates
Production year
Manufacturer
Risk: electrocution.
Consequence: Death.
Do not use the device
while taking a bath or a shower
Socket for low safety voltage
Keep away from sunlight
the device is