Technical Data; Applied Parts - FLAEM Air Pro 3000 Standard Version Mode D'emploi

TECHNICAL DATA

Mod. P0712EM F3000 Standard Version
Power source:
Fuse:
Max Pressure:
Compressor air delivery:
Noise (at 1 m):
Operation:
Operating conditions:
Storage conditions:
Operating/storage
atmospheric pressure:
Compliant with Directive 93/42 EEC
Apparatus size:
Weight:

APPLIED PARTS

The applied parts of type BF are:
TECHNICAL SPECIFICATIONS RF7 Dual Speed Plus Nebulizer
Minimum fill volume:
Maximum fill volume:
sYMBOLs
Class II device
Important: check the operating instructions
Keep dry
When the device is turned off, the
"ON"
switch interrupts compressor operation
only on one of the two power supply
"OFF"
phases.
Complies with: European standard EN
10993-1 "Biological Evaluation of Medical
Devices" and European Directive 93/42/EEC
"Medical Devices"
Serial number of device
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 op-
eration of electrical medical devices. For further information visit www.flaemnuova.it or www.flaem.it Flaem reserves the
right to make technical and functional changes to the product without notice.
230 V ~ 50 Hz / 210 VA
1 x T2A 250V
3,5±0,5 bar
14 l/min approx.
55 dB (A) approx.
Continuous
Temperature min. 5 °C; max. 35 °C
Air humidity min. 10%; max. 95%
Temperature min. -25 °C; max. 70 °C
Air humidity min. 10%; max. 95%
min. 690 hPa; max. 1060 hPa
0051
26 (W) x 12 (D) x 23,5 (H) cm
2,2 kg
(C1,C2,C3,C4)
2 ml
8 ml
17
Tipe BF applied part
Alternate current
CE Medical Marking ref. Dir. 93/42
0051
EEC and subsequent amendments
Hazard: electrocution.
Consequence: Death.
Do not use device while taking a
bath or shower
Manufacturer