FLAEM Delphinus Manual De Instrucciones página 7

TECHNICAL SPECIFICATIONS
Mod. DELPHINUS F1000
Voltage: 230V~ 50Hz 140VA
In conformity Dir. 93/42/EEC
with:
Approvals:
Max Pressure: 2.6 ± 0.4 bar
Compressor air output: 10 LPM approx
Noise level (at 1 m): 56 dB (A) approx
Operation: Continuous use
Dimensions 18(W)x30(D)x10(H) cm
Weight 2.100 Kg
Operating conditions:
Storage conditions:
Operating/storage atmospheric pressure: min. 69KPa; máx. 106KPa
APPLIED PARTS
Type BF applied parts include: (C1,C2,C3,C4)
RF6 PLUS NEBULIZER
Medication minimum capacity : 2 ml
Medication maximum capacity: 8 ml
Operating
pressure
bar
0.9
(1)Data detected according to Flaem I29-P07.5 internal procedure. (2)In vitro characterization certified by TÜV Rheinland Product Safety GmbH -
Germany in compliance with the new European Standard for aerosol therapy units, Standard EN 13544-1, ANNEX CC. Further details are available on
request.
Disposal: In conformity with Directive 2002/96/EC, the symbol shown on the appliance to be
disposed of indicates that this is considered as waste and must therefore undergo "sorted waste
collection". The user must therefore take (or have taken) the above waste to a pre-sorted waste
collection centre set up by the local authorities, or else give it back to the dealer when purchasing a
new appliance of the same type. Pre-sorted waste collection and the subsequent treatment, recovery
and disposal operations favour the production of appliances made of recycled materials and limit
the negative effects of any incorrect waste management on the environment and public health. 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 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.
115V~ 60Hz 180VA
Temperature: min 10°C; max 40°C
Air humidity: min 10%; max 95%
Temperature: min -25°C; max 70°C
Air humidity: min 10%; max 95%
BREATHABLE
(2)
MMAD FRACTION
(2)
μm < 5 μm (FPF)
3.2
220V~ 60Hz 160VA
open
%
valve-holder MAX
73 0.42
5
100V~ 50/60Hz
DELIvERY
(1)
ml/min
closed
valve-holder MIN
0.15