Electromagnetic Compatibility; Packaging Disposal - FLAEM NebulFlaem 4.0 Bedienungsanleitung

TECHNICAL SPECIFICATIONS
Mod. CONDOR F2000
Voltage: 230V~ 50Hz 210VA
Max pressure:
Compressor air delivery:
Noise (at 1 m):
Operation:
Operating Conditions:
Temperature:
Air humidity:
Atmospheric pressure:
Storage conditions:
Temperature:
Air humidity:
Atmospheric pressure:
Dimensions:
Weight:
APPLIED PARTS
Type BF applied parts are:
RF9
Minimum medication capacity:
Maximum medication capacity:
Operating pressure (with neb.):

ELECTROMAGNETIC COMPATIBILITY

This device was designed to satisfy the currently required requisites for electromagnetic compatibility (EN 60601-
1-2). Electro-medical devices require particular care during installation and use relative to EMC requirements. Users
are therefore requested to install and/or use these devices following the manufacturer's specifications. There is a risk
of potential electromagnetic interference with other devices. RF mobile or portable radio and telecommunications
devices (mobile telephones or wireless connections) can interfere with the functioning of electro-medical devices.
For further information visit our website www.flaemnuova.it. The Medical Device may be subject to electromagnetic
interference if other devices are used for specific diagnosis or treatments. Flaem reserves the right to make technical
and functional modifications to the product with no prior warning.
DEVICE DISPOSAL
In compliance with the Directive 2012/19/EC, the symbol printed on the device shows that the device to be
disposed of is considered waste and must therefore be an item of ''differentiated collection'' . Consequently, the
user must take it (or have it taken) to the designated collection sites provided by the local authorities, or turn
it in to the dealer when purchasing an equivalent new device. Differentiated waste collection and the subsequent
treatment, recycling and disposal procedures promote the production of devices made with recycled materials and
limit the negative effects on the environment and on health caused by potential improper 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.

PACKAGING DISPOSAL

Product box
20
PAP
Heat shrink film accessories
05
PP
115V~ 60Hz
3.5 ± 0.3 bar
approx 14 l/min
approx 55 dB (A)
Continuous
min 10°C; max 40°C
min 10%; max 95%
min 69KPa; max 106KPa
min -25°C; max 70°C
min 10%; max 95%
min 69KPa; max 106KPa
20 (W) x 29,5 (D) x 10 (H) cm
2.400 Kg
patient accessories (C2, C3, C4, C5)
2 ml
8 ml
approx. 1.30 bar
Product packaging bag and
04
Tube packaging bag
LDPE
8
220V~ 60Hz 100V~50/60Hz