1
6
TE
C
HNI
CA
L FE
A
TURES
Mod. P0703EM F400
Voltage:
23
0V~
5
0Hz 1
3
0V
A
11
5
V ~
6
0Hz
22
0V ~
6
0Hz
Safety certifications:
Max pressure:
C
ompressor air output:
Sound level (at 1 m):
Operation:
1
.8
± 0
.3
bar
9 l/min approx
54
dB (
A
) approx
C
ontinuous
Operating conditions:
Temperature:
RH
A
ir humidity:
A
tmospheric pressure:
min 10°
C
; max
4
0°
C
min 10%; max 9
5
%
min
6
9KPa; max 10
6
KPa
Storage conditions:
Temperature:
RH
A
ir humidity:
A
tmospheric pressure:
min -
25
°
C
; max 70°
C
min 10%; max 9
5
%
min
6
9KPa; max 10
6
KPa
Dimensions (W)x(D)x(H):
Weight:
19x
2
7x11 cm
1
.
700 Kg
A
PPLIED P
A
RTS
Type BF applied parts are:
patient accessories (
C2
,
C3
,
C4
,
C5
,
C6
)
RF7 Dual Speed nebulizer
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with neb
.
):
2
ml
8
ml
0
.
7 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.
7
8
μm
(2)
Breathable fractions < 5 μm (FPF):
54.4
%
63
%
(1) Data detected according to Flaem I
2
9-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 1
3544
-1:
2
007 +
A
1 European Standard
for aerosol therapy devices Standard
.
More details are available on request
.
DEVI
C
E DISPOS
A
L
In compliance with the Directive
2
01
2
/19/E
C
, 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''
.
C
onsequently, 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
2
01
2
/19/E
C
of the European member state or of the country in
which the product is disposed of
.
