Technical Data - FLAEM RespinAir P0611EM F1000 Mode D'emploi

TECHnICAL DATA

Mod.: P0611EM F1000
Voltage: 230V~ 50Hz 140VA 115V ~ 60Hz 220V ~ 60Hz 100V ~ 50/60Hz
Safety certifications:
Max Pressure:
Compressor air output:
Noise level (at 1 m):
Operation:
Dimensions (L)x(P)x(H):
Weight:
Operating conditions:
Temperature:
Air humidity:
Atmospheric pressure:
Storage conditions:
Temperature:
Air humidity:
Atmospheric pressure:
APPLIED PArTS
Type BF applied parts include:
rF7 DUAL SPEED PLUS nebulizer
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with neb.):
Delivery:
(1)
MMAD:
(2)
Breathable fractions < 5 μm (FPF):
(2)
data detected according to Flaem I29-P07.5 internal procedure
(1)
In vitro characterization certified by TÜV Rheinland Product Safety GmbH - Germany in compliance with the new European Standard for aerosol
(2)
therapy units, Standard EN 13544-1, ANNEX CC. Further details are available on request.
DEVICE DISPOSAL
In conformity with Directive 2002/96/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 deliver (or have delivered) the above waste to an appropriate waste collection
centre provided by the local authorities, or deliver it 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
to the environment and public health due to incorrect waste management. The unlawful disposal of the
product by the user could result in administrative fines as provided by the laws transposing Directive
2002/96/EC of the European member state or of the country in which the product is disposed of.
ELECTrOMAgnETIC COMPATIBILITy
This device has been designed to satisfy requirements currently required for electromagnetic
compatibility (EN 60 601-1-2:2007). Electrical medical devices require special care. During installation and
use with respect to EMC requirements, it therefore required that they be installed and/or used according
to the manufacturer's specification. Potential risk of electromagnetic interference with other devices, in
particular with other devices for analysis and treatment. Radio and mobile telecommunications devices
or portable RF (mobile phones or wireless connections) may interfere with the operation of electrical
medical devices. For further information visit www.flaemnuova.it. Flaem reserves the right to make
technical and functional changes to the product without notice.
2.6 ± 0.4 bar
10 l/min approx
54 dB (A) approx
Continuous use
16x16x10 cm
1.45 Kg
min 10°C; max 40°C
min 10%; max 95%
min 69KPa; max 106KPa
min -25°C; max 70°C
min 10%; max 95%
min 69KPa; max 106KPa
(C2,C3,C4)
2 ml
8 ml
0.90 bar
Speed selector C1.4
in pos Max
0.53 ml/min approx.
2.53 μm
79.6%
6
Speed selector C1.4
in pos Min with valve
0.23 ml/min approx.
2.72 μm
77.8%