Technical Data - FLAEM Lella Manual De Instrucciones

TECHNICAL DATA

Voltage:
Safety certifications:
Max Pressure:
Compressor air output:
Dimensions (L)x(P)x(H)
Weight
Noise level (at 1 m):
Operation:
APPLIED PARTS
Type BF applied parts include:
RF6 BASIC Nebulizer
2
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 GmbH - Germany in compliance with the new European Standard for aerosol therapy
(2)
units, Standard EN 13544-1. Further details are available on request.
NASAL SHOWER SPECIFICATIONS Mod.: Rhino Clear®
Capacity:
10 ml dispensing time
(1)
MMD
(2)
% <10 μm
(2)
Tests carried out with 0,9% NaCl physiological solution according to Flaem internal procedure
(1)
Data gathered with Laser Malvern Mastersizer system (in a certified laboratory)
(2)
Operating conditions:
Temperature: min 10°C; max 40°C
Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
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 60601-1-2:2007). 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.
230V~ 50Hz 140VA
2,6 ± 0,4 bar
10 l/min approx
21x16x13 cm
1.600 Kg
55 dB (A) approx
Continuous use
patient accessories (C2,C3,C4,C5.1A-C5.1B-C5.1C)
2 ml
8 ml
0.8 bar
drug 10 ml maximum
2' 10''
48 μm
3.2%
115V ~ 50Hz
Mod. High speed
0.42 ml/min approx.
3.6 μm
67%
Storage conditions:
Temperature: min -25°C; max 70°C
Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
14
220V ~ 50Hz
Mod. standard
0.32 ml/min approx.
3.6 μm
66%