INFORMATION ON RESTRICTIONS OR INCOMPATIBILITIES WITH CERTAIN SUBSTANCES
• Interactions: The materials used in the device are biocompatible materials and comply with
statutory regulations, however possible allergic reactions cannot be completely excluded. • Use the
medicine as soon as possible once it has been opened and avoid leaving it in the nebuliser; once ther-
apy has ended, do not leave the medicine inside the nebuliser and proceed with hygienic preparation.
COMPRESSOR UNIT SPECIFICATIONS. MODEL: CONDOR F2000
Power supply: 230V~ 50Hz 210VA
Max. pressure: 3.5 ± 0.5 bar
Air flow to compressor: 14 l/min approx
NEBULIZER TECHNICAL SPECIFICATIONS.
RF9 Nebuliser
Minimum drug capacity: 2 ml
TECHNICAL SPECIFICATIONS OF DEVICE. Model: CONDOR F2000 combined RF9-1
Operating pressure (with neb.):
RESPIRATORY
SYSTEM
CONFIGURATION
BOWL
MMAD (μm)
Output rate (ml/min')
Respirable fraction < 5
μm (FPF) %
(1) Data collected according to Flaem's internal procedure. (2) In vitro characterisation performed by TÜV Rheinland
Italia S.r.l. in cooperation with the University of Parma. More details are available on request. (3) Data calculated on the
basis of the values obtained with the Malvern Spraytec and compared with the values of the tests performed at the
University of Parma.
APPLIED PARTS. Type BF applied parts are: patient accessories (B3, B3.2, B4, B5)
Weight: 2.400 Kg
ENVIRONMENTAL CONDITIONS
Operating conditions:
Ambient temperature: Between +10°C and +40°C Ambient temperature: Between -25°C and +70°C
Relative air humidity: Between 10% and 95%
Atmospheric pressure: Between 69 KPa and 106 KPa Atmospheric pressure: Between 69 KPa and 106 KPa
DURATION
Model: CONDOR F2000 (Compressor unit). Service life 2000 hours.
Model: RF9-1(Nebuliser and accessories). The expected average life is 1 year, however it is advisable
to replace the nebuliser every 6 months during intensive use (or sooner if the nebuliser is clogged) to
ensure maximum therapeutic effectiveness.
Noise level (at 1 m): 55 dB (A) approx
Operation: Continued
Dimension: 20(L) x 29,5(D) x 10(H) cm
Maximum drug capacity: 8 ml
1.30 bar.
UPPER AIRWAYS
Oropharyngeal
Tracheobronchial
tract
Without
Selector in
Selector (Fig. 1)
position 1 (Fig. 2)
5.80
(3)
0.75
(1)
40.3
(3)
Model: RF9-1
LOWER AIRWAYS
Pulmonary
tract
tract
Selector in
position 2 (Fig. 3)
4.67
3.62
(2)
0.54
0.51
(1)
54.4
66.3
(2)
Storage and transport conditions:
Relative air humidity: Between 10% and 95%
14
Peripheral
tract
Selector in
position 3 (Fig. 4)
2.56
(2)
(2)
0.38
(1)
(1)
82.2
(2)
(2)
Be
sec
on
(so
mu
wi
1. I
ap
2.
(B2