Flaem NOVAMA NELLA P0406EM F400, Руководство по эксплуатации

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DEVICE DISPOSAL
In compliance with Directive 2012/19/EC, the symbol printed on the device shows that the device being disposed
of is considered waste and must therefore be ''collected separately''. 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. Separate 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. If the user disposes of the product in an unauthorised
manner, administrative penalties shall be applied according to the transposition laws of directive 2012/19/EC of the
member state or country where the product is disposed of.
with open valve holder
MAX (approx.)
with closed valve holder
MIN (approx.)
(1)
Delivery:
approx. 0.32 l/min approx. 0.19 l/min
(2)
MMAD:
3.67 μm 3.34 μm
(2)
Breathable fraction < 5 μm (FPF): 66% 69.2 %
(1)
Data recorded according to internal Flaem procedure I29-P07.5
(2)
In vitro characterisation performed at TÜV Rheinland Product GmbH - Germany in compliance with the new European Standard for Aerosol therapy devices EN
13544-1, ANNEX CC. Further details are available on request.
TECHNICAL SPECIFICATIONS
DEVICE Mod. P0406EM F400
Power supply: 230V~ 50Hz 130VA
Max pressure: 1.8 ± 0.3 bar
Compressor air delivery: approx. 9 l/min
Dimensions: 21X16X13 cm
Weight: 1.73 Kg
Noise (at 1 m): approx. 55 dB (A)
Continuous operation
Approvals:
APPLIED PARTS
Type BF applied parts are: patient accessories (C2, C3, C4, C5)
Nebuliser RF6 PLUS
Minimum medication capacity: 2 ml
Maximum medication capacity: 8 ml
Operating pressure (with neb.): 0.6 bar