Flaem AirMate P0504EM F400, Инструкция по эксплуатации, Страница: 18 / 68

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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.
TECHNICAL FEATURES
Mod. P0504EM F400
Voltage:
230V~ 50Hz
130VA
115V ~ 60Hz 220V ~ 60Hz
Safety certifications:
Max pressure:
Compressor air output:
Sound level (at 1 m):
Operation:
1.8 ± 0.3 bar
9 l/min approx
54 dB (A) approx
Continuous
Operating conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
min 10°C; max 40°C
min 10%; max 95%
min 69KPa; max 106KPa
Storage conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
min -25°C; max 70°C
min 10%; max 95%
min 69KPa; max 106KPa
Dimensions (W)x(D)x(H):
Weight:
16 x 20 x 12 cm
1.500 Kg
APPLIED PARTS
Type BF applied parts are: patient accessories (C2, C3, C4, C5)
RF8 Dual Speed nebuliser
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with neb.):
2 ml
8 ml
0.8 bar
C1.2.3 speed selector
in Max pos in pos Min
(1) Delivery: 0.40 ml/min approx. 0.19 ml/min approx.
(2)
MMAD: 4.48 μm 4.01 μm
(2)
Breathable fraction < 5 μm (FPF): 55.5 % 61.1 %
(1) Data recorded according to internal Flaem procedure I29-P07.5.
(2) In vitro characterization certified by TÜV Rheinland LGA Products GmbH - Germany in compliance with
European Standard for Aerosol therapy apparatuses EN 13544-1. Further details are available on request.