20
Specifications
Technical data
Product name
: Omron Ultrasonic Nebuliser
Model :
NE-U17
(NE-U17-E)
Power source
: 230 VAC, 50 Hz
Power consumption
: Approx. 80 VA
Fuse :
T2A
L250V
Ultrasonic frequency
: Approx. 1.7 MHz
Particle size
: * MMAD 4.4 µm (MMAD=Mass Median Aerodynamic Diameter)
Nebulisation rate
: ** Approx. 0 to 3 ml adjustable
Sound
: ** Less than 45 dB
Air volume
: Maximum of 17 l/min
Amount of cooling water
: Approx. 375 ml
Capacity of medication cup : Approx. 150 ml (min. 5 ml)
External dimensions
: Approx. 276 (W) x 243 (H) x 226 (D) mm
Weight of the main unit
: Approx. 4.0 kg
Protection class
: Class I
Operating condition
: Continuous
Operating temperature /
: 5°C to 40°C (41°F to 104°F) / 30 to 85% RH
humidity
Storage temperature /
: -20°C to 60°C (-4°F to 140°F) / 10 to 95% RH / 700 to 1060 hPa
humidity / air pressure
Accessories included
: Inhalation hose M (with a cuff, 70 cm), Mouthpiece set, 2 Medication cups,
Power cord, Instruction manual (with warranty card)
Result of cascade impactor measurements for particle size
0
50
100
0.1
1
10
100
individual
mean
Cumulative % particle mass of sodium fluoride under size
Dp (µm)
Cum
ulativ
e Undersiz
e %
* Independently measured at SolAero Ltd., Canada, Dr. John Dennis, according to EN13544-1:2007.
** Measured by OMRON HEALTHCARE Co., Ltd..
Notes:
• Subject to technical modification without prior notice.
• This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan.
• The device may not work if the temperature and voltage conditions are different to those defined in the specifications.
• Do not use the device where it may be exposed to flammable gas.
• The Nebulisation rate is measured with saline 0.9% solution at 23°C and can vary with medication and ambient conditions.
• The distribution of particle size is measured with 2.5% NaF solution and can vary with medication and ambient conditions.
• Performance may vary with drugs such as suspensions or high viscosity. See drug supplier’s data sheet for further details.
• See web site of OMRON HEALTHCARE EUROPE to update technical information.
URL: www.omron-healthcare.com
• This device fulfils the provisions of the EC directive 93/42/EEC (Medical Device Directive) and the European Standard
EN13544-1:2007, Respiratory therapy equipment - Part1: Nebulising systems and their components.
Symbols:
=Type B
Read the instruction
manual carefully
EN
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14/12/2010 13:49:29
