Disposal Of Device; Electromagnetic Compatibility - FLAEM Wi.Neb Go Manual De Instrucciones

RF7 PLUS Nebulizer
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with nebulizer):
(1)
Delivery:
(2)
MMAD:
(2)
Breathable fractions < 5 μm (FPF):
(1)
Data detected according to Flaem I29-P07.5 internal procedure.
University of Parma and in compliance with the EN 13544-1: 2007 + A1 European Standard for aerosol therapy devices Standard. More details are
available on request.
Use only power adaptor mod. UME318-1215 (cod. 13014)
Primary:
Secondary:
Universal power adaptor (USA alternative)
Use only power adaptor mod. UML318-1215 (cod. 13373)
Primary:
Secondary:
Power cord for 12V DC cigarette lighter receptacle
If the fuse inside the connection plug blows, replace with 3A.

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. Risk of potential electromagnetic
interference with other devices. Mobile or portable RF radio and telecommunication devices (mobile phones or wireless
connections) may interfere with the operation of medical devices. For more information, visit the website www.flaemnuova.
it. The appliance may be susceptible to electromagnetic interference in the presence of other devices used for specific
diagnoses or treatments. Flaem reserves the right to make technical and functional changes to the product without prior
notice.
2 ml
8 ml
approx. 0.7 bar
Min With valve 0.18 ml/min
Max: approx. 0.42 ml/min
Min With valve 2.95 μm
Max: 2.44 μm
Min With valve 74.7%
Max: 80.7%
(2)
In vitro testing performed by TÜV Rheinland Italia S.r.l. in collaboration with the
100/240V~ 50/60Hz
12V DC 1.5 A
100/240V~ 50/60Hz
12V DC 1.5 A
ENGLISH
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