Device Disposal; Electromagnetic Compatibility - FLAEM ASPIRA P1211EM Gebrauchsanweisung

SYMBOLS
Class II device
Type BF applied part
Attention: check the instructions for use
Single use
Alternating current
Ethylene oxide sterilisation
Device serial number

DEVICE DISPOSAL

In compliance with the Directive 2002/96/CE, the symbol printed on the device shows that the device to be
disposed of is considered waste and must therefore be an item of "differentiated collection". 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. Unauthorised disposal of the product by the user shall result in the application of administrative
penalties, of which article 50 and the subsequent revisions of Italian Legislative Decree no. 22/1997.

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
"ON"
"OFF"
EEC ref. Directive 93/42 CE medical mark and
0051
subsequent revisions
Without latex
Production year
Manufacturer
TÜV Certification
ref. ISO 10079-1
15
When the device is switched off, the on/off
switch stops compressor function in only
one phase of the two-phase power supply.