Disposal Of Device; Electromagnetic Compatibility - Chiesi Clenny A Family Care 4 Evolution Bedienungsanleitung

SYMBOLS
CE Medical Marking ref.
Dir. 93/42 EEC and subsequent
amendments
Class II device
Important: check the operating
instructions
Switch
"ON"
Switch
"OFF"
Minimum and maximum
atmospheric pressure
Complies with: European standard
EN 10993-1 "Biological Evaluation
of Medical Devices" and European
Directive 93/42/EEC "Medical
Devices". Phthalates free. In
conformity with Reg. (EC) no.
1907/2006

DISPOSAL OF DEVICE:

In conformity with Directive 2012/19/EC, the symbol shown on the device to be
disposed of indicates that it is considered as waste and is therefore subject to
"sorted waste collection". The user must therefore take (or have taken) the above
waste to a pre-sorted waste collection centre set up by the local authorities, or else
give it back to the dealer when purchasing a new appliance of the same type. Pre-sorted
waste collection and the subsequent treatment, recovery and disposal operations favor
the production of appliances made of recycled materials and Iimit the negative effects
of any incorrect waste management on the environment and public health. 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 60601-1-2). 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. 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 the manufacturer's website. The Medical Device may be subject
to electromagnetic interference if other devices are used for specific diagnosis or
treatments. The manufacturer reserves the right to make technical and functional
modifications to the product with no prior warning.
When you shut off the
device, the switch will
interrupt the compressor
function only on one of the
two power phases
Serial number of device
Manufacturer
Type BF applied part
Alternating current
Minimum and maximum room
temperature
Minimum and maximum air moisture
Enclosure protection rating: IP21.
(Protected against solid bodies over
IP21
12 mm. Protected against access with
a finger. Protected against vertically
falling water drops).
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