9
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.
Mod. NEBULAIR
Voltage:
230V~ 50Hz
210VA
115V~ 60Hz
230VA
220V~ 60Hz
230VA
100V~50/60Hz
230VA
Approvals:
Max pressure:
3.5 ± 0.5 bar
Compressor air delivery:
approx 14 l/min
Noise (at 1 m):
approx 55 dB (A)
Operation:
Continuous
Operating Conditions:
Temperature:
min 10°C; max 40°C
Air humidity:
min 10%; max 95%
Atmospheric pressure:
min 69KPa; max 106KPa
Storage conditions:
Temperature:
min -25°C; max 70°C
Air humidity:
min 10%; max 95%
Atmospheric pressure:
min 69KPa; max 106KPa
Dimensions:
20 (W) x 30 (D) x 10 (H) cm
Weight:
2.400 Kg
APPLIED PARTS
Type BF applied parts are:
patient accessories (C2, C3, C4, C5)
RF7 Dual Speed Plus Nebuliser
Minimum medication capacity:
2 ml
Maximum medication capacity:
8 ml
Operating pressure (with neb.):
approx. 1.30 bar
TECHNICAL SPECIFICATIONS
C1.4 speed selector
in Max pos
in Min pos with valve
(1)
Delivery:
approx. 0.65 ml/min
approx. 0.29 ml/min
(2)
MMAD:
2.38 μm
2.21 μm
(2)
Breathable fraction < 5 μm (FPF):
81.5%
84.2%
(1) data recorded according to internal Flaem procedure I29-P07.5.
(2) In vitro characterization certified by TÜV Rheinland LGA Products GmbH - Germany in compliance with European
Standard for Aerosol therapy apparatuses EN 13544-1. Further details are available on request.
