Device Disposal; Electromagnetic Compatibility - FLAEM Aspira go Mode D'emploi

SYMBOLS
Class II device
Type BF applied part
Attention: check the instructions for use
Single use
More vacuum
Less vacuum
Socket for low safety voltage
Ethylene oxide sterilisation
Device serial number
TÜV approval ref. ISO 10079-1
Keep away from sunlight

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 currently required requisites for electromagnetic compatibility (EN
60 601-1-2:2007). 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) can interfere with the functioning of electro-medical devices. For further
information visit our website www.flaemnuova.it.
Flaem reserves the right to make technical and functional modifications to the product with no prior warning.
Risk: electrocution.
Consequence: Death.
Do not use the device
while taking a bath or a shower
Switch on
Switch off
Direct current
Alternating current
CE Marking medical ref. Dir 93/42
0051
EEC and subsequent updates
Without latex
Production year
Manufacturer
18