Technical Data; Device Disposal; Electromagnetic Compatibility - NEWMED Levita Gebrauchsanweisung

TECHNICAL DATA

Model: NM-F700
Voltage:
Max pressure:
Compressor air output:
Sound level (at 1 m):
Operation:
Operating conditions:
Storage conditions:
Dimensions (W)x(D)x(H)
Weight:
APPLIED PARTS
Type BF applied parts are:
RF8 NEBULIZER
Medication Medication
minimum maximum
capacity capacity
ml ml
2
(1) Values measured according to Manufacturer' s internal procedure I29-P07.5 Delivery rate values can change depending on the patient' s respiratory capacity.
(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.
230V~ 50Hz 140VA
2.6 ± 0.4 bar
10 l/min approx
Approx. 57 dB (A) with open cover
approx. 54 dB (A) with closed cover
continuous
Temperature: min 10°C; max 40°C
RH Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
Temperature: min -25°C; max 70°C
RH Air humidity: min 10%; max 95%
Atmospheric pressure: min 69KPa; max 106KPa
270x180x110 cm
1.7 Kg
patient accessories (C2, C3, C4, C5)
(1)Operating
pressure
bar
8
1.15
(1)Delivery ml/min (2)MMAD
(μm)
(approx)
max max max
0.44 0.28 4.12
(2)EINATEMBARE
FRAKTIONEN < 5
μm (FPF) %
max max max
3.69 59.8 64.2