Packaging Disposal; Device Disposal - FLAEM AirMate Mode D'emploi

SYMBOLS
CE Medical Marking ref. Dir. 93/42
EEC and subsequent amendments
Class II device
Important: check the operating
instructions
"OFF" for part of equipment
"ON" for part of equipment
Complies with: European standard
EN 10993-1 "Biological Evaluation of
Medical Devices" and European Di-
rective 93/42/EEC "Medical Devices".
Phthalates free. In conformity with
Reg. (EC) no. 1907/2006
Temperature limit

PACKAGING DISPOSAL

Product box
20
PAP
05 Heat shrink film accessories
PP

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 an item of ''differentiated collection'' . Consequently, the user must take it (or
have it taken) to the designated 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.
Certification TÜV
Serial number of device
Manufacturer
Type BF applied part
Alternating current
Enclosure protection rating: IP21.
(Protected against solid bodies over
IP21
12 mm. Protected against access
with a finger.Protected against
vertically falling water drops).
Humidity limit
Atmospheric pressure limit
Tube packaging bag
04
LDPE
Packaging bag for accessories
02
bag
HDPE
15