Applied Parts; Electromagnetic Compatibility - FLAEM NebulAIR Bedienungsanleitung

Max Pressure:
Compressor air output:
Noise level (at 1 m):
Operation:
Dimensions
Weight
Operating conditions:
Storage conditions:
Operating/storage
atmospheric pressure:

APPLIED PARTS

Type BF applied parts include:
RF6 Plus NEBULIZER
Medication minimum capacity :
Medication maximum capacity:
Operating
pressure
bar
1.2
(1) Data shown is in accordance with Flaem Nuova internal procedure I29-P07.5.
(2) In vitro testing certified by TÜV Rheinland Product Safety GmbH - Germany in compliance with the European Standard
EN 13544-1. More details are available on request.
Disposal: In conformity with Directive 2012/19/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 2012/19/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 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.
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3.5 ± 0.5 bar
14 LPM approx
55 dB (A) approx
Continuous use
20(W)x30(D)x10(H) cm
2.400 Kg
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%
min. 69KPa; máx. 106KPa
(C1,C2,C3,C4)
2 ml
8 ml
BREATHABLE
(2)
MMAD FRACTION
(2)
μm < 5 μm (FPF)
2.8
open
valve-holder
%
MAX
76 0.54 approx
7
DELIVERY
(1)
ml/min
closed
valve-holder
MIN
0.21 approx