Technical Data; Інструкціяз Використання - NEWMED FIORE Gebrauchsanweisung

TECHNICAL DATA

Model NM-F400
Voltage: 230V~ 50Hz 130VA
Max pressure: 1.8 ± 0.3 bar
Compressor air output: 9 l/min approx
Sound level (at 1 m): 54 dB (A) approx
Operation: continuous
Operating conditions: Temperature: min 10°C; max 40°C
RH Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
Storage conditions: Temperature: min -25°C; max 70°C
RH Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
Dimensions (W)x(D)x(H) 16x16.5x11.5 cm
Weight: 1.3 Kg
APPLIED PARTS
Type BF applied parts are: patient accessories (C2, C3, C4, C5)
RF8 NEBULIZER
Medication Medication Operating
minimum minimum pressure
capacity capacity bar
ml ml
2 8
0.8
(
1)
(1) Data shown is in accordance with Manufacturer internal procedure I29-P07.5.
(2) In vitro characterization certified by TÜV Rheinland LGA Product GmbH - Germany in compliance with the
European Standard EN 13544-1, ANNEX CC for nebulizing system. More details are available on request.
DEVICE DISPOSAL
In conformity with Directive 2012/19/EC, the symbol shown on the device to be disposed of indicates that it is considered as waste
and is therefore subject to "sorted waste collection". The user must therefore deliver (or have delivered) the above waste to an
appropriate waste collection centre provided by the local authorities, or deliver it to the dealer when purchasing a new appliance
of the same type. Presorted waste collection and the subsequent treatment, recovery and disposal operations favor the production
of appliances made of recycled materials and Iimit the negative effects to the environment and public health due to incorrect
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.
ELECTROMAGNETIC COMPATIBILITY
This device has been designed to satisfy requirements currently required for electromagnetic compatibility (EN 60 601-1-2:2007). Electrical medical
devices require special care during installation and use with respect to EMC requirements. It is 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.
new-med.at. Manufacturer reserves the right to make technical and functional changes to the product without notice.
NEWMED GmbH Absbergasse 27, Stiege 7, 1100, Wien, Austria
Delivery MMAD BREATHABLE
ml/min (μm) FRACTIONS < 5
(approx) μm (FPF) %
0.40 4.48 55.5
( ( (
1) 1) 1)
ІНСТРУКЦІЯ
З ВИКОРИСТАННЯ
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