Technical Data - FLAEM P0406EM F700 Bedienungsanleitung

TECHNICAL DATA

Mod. P0406EM F700
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 2012/19/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 2012/19/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'
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
12
220V ~ 50Hz
Mod. standard
0.32 ml/min approx.
3.6 μm
66%