TECHNICAL FEATURES
Mod. P0504EM F400
Voltage:
Safety certifications:
Max pressure:
Compressor air output:
Sound level (at 1 m):
Operation:
Operating conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
Storage conditions:
Temperature:
RH Air humidity:
Atmospheric pressure:
Dimensions (W)x(D)x(H):
Weight:
APPLIED PARTS
Type BF applied parts are:
RF8 nebuliser
Medication minimum capacity:
Medication maximum capacity:
Operating pressure (with neb.):
Delivery:
(1)
MMAD:
(2)
Breathable fraction < 5 μm (FPF):
(2)
(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.
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.
230V~ 50Hz
130VA
1.8 ± 0.3 bar
9 l/min approx
54 dB (A) approx
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
16 x 20 x 12 cm
1.500 Kg
patient accessories (C2, C3)
2 ml
8 ml
0.8 bar
7
115V ~ 60Hz
0.40 ml/min approx.
4.48 μm
55.5%
220V ~ 60Hz