Flaem Neb-aid - Technical Features; Disposal of Device

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 eects
of any incorrect waste management on the environment and public health. The unlawful
disposal of the product by the user could result in administrative nes 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.
TECHNICAL FEATURES
Mod. P0603EM F400
Voltage: 230V~ 50Hz 130VA 115V ~ 60Hz 220V ~ 60Hz
Safety certications:
Max pressure:
Compressor air output:
Sound level (at 1 m):
Operation:
1.8 ± 0.3 bar
9 l/min approx
54 dB (A) approx
Continuous use
Operating conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
min 10°C; max 40°C
min 10%; max 95%
min 69KPa; max 106KPa
Storage conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
min -25°C; max 70°C
min 10%; max 95%
min 69KPa; max 106KPa
Dimensions (W)x(D)x(H):
Weight:
18x14x13 cm
1.300 Kg
APPLIED PARTS
Type BF applied parts are: patient accessories (C2, C3, C4, C5)
RF7 Dual Speed nebulizer
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with neb.):
2 ml
8 ml
0.65 bar
Speed selector C1.4
Max Min
(1)
Delivery: 0.55 ml/min approx. 0.25 ml/min approx.
(2)
MMAD: 4.58 μm 3.78 μm
(2)
Breathable fractions < 5 m (FPF): 54.4% 63%
(1) Data detected according to Flaem I29-P07.5 internal procedure. (2) In vitro testing performed by TÜV Rheinland Italia
S.r.l. in collaboration with the University of Parma and in compliance with the EN 13544-1: 2007 + A1 European Standard
for aerosol therapy. More details are available on request.
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