Instruction Manual

4
5. Malfunctions and Actions to take
The device cannot be switched on
 Make sure that the plugs are properly inserted in the power
outlet and the device.
The nebuliser functions poorly or not at all
 Ensure the air tube 8 is correctly connected at both ends.
 Ensure the air tube is not squashed, bent, dirty or blocked. If
necessary, replace with a new one.
 Ensure the nebuliser 7 is fully assembled and the vaporiser
head 7-a is placed correctly and not obstructed.
 Ensure the required medication has been added.
 Ensure the air filter AM is mounted properly (device is noisy).
6. Guarantee
This device is covered by a 2 year guarantee from the date of
purchase. During this guarantee period, at our discretion, Microlife
will repair or replace the defective product free of charge.
Opening or altering the device invalidates the guarantee.
The following items are excluded from the guarantee:
 Transport costs and risks of transport.
 Damage caused by incorrect application or non-compliance
with the instructions for use.
 Damage caused by leaking batteries.
 Damage caused by accident or misuse.
 Packaging/storage material and instructions for use.
 Regular checks and maintenance (calibration).
 Accessories and wearing parts: Batteries, nebuliser, masks,
mouthpiece, nose piece, tube, filters, micro USB cable, AC
adapter (optional).
Should guarantee service be required, please contact the dealer
from where the product was purchased, or your local Microlife
service. You may contact your local Microlife service through our
website:
www.microlife.com/support
Compensation is limited to the value of the product. The guarantee
will be granted if the complete product is returned with the original
invoice. Repair or replacement within guarantee does not prolong
or renew the guarantee period. The legal claims and rights of
consumers are not limited by this guarantee.
7. Technical Specifications
This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Class II device as regards protection against electric shocks.
Nebuliser, mouthpiece and masks are type BF applied parts.

Do not try to clean the filter for reusing it.

The air filter shall not be serviced or maintained while in use
with a patient.
Only use original filters! Do not use the device without filter!
Nebulisation rate: 0.25 ml/min. (NaCI 0.9%)
Particle size: 65% < 5 µm
2.9 µm (MMAD)
Operating pressure: 0.25 - 0.5 bar
Acoustic noise level: 45 dBA
AC adapter: Input: 100-240VAC 50/60Hz 0.5A
Output: 5V DC 2A
Nebuliser capacity: min. 2 ml; max. 6 ml
Residual Volume: 0.8 ml
Operating limits: 30 min. On / 30 min. Off
Operating condi-
tions:
10 - 40 °C / 50 - 104 °F
10 - 95 % relative maximum humidity
700 - 1060 hPa Atmospheric pressure
Storage and shipping
conditions:
-20 - +60 °C / -4 - +140 °F
10 - 95 % relative maximum humidity
700 - 1060 hPa Atmospheric pressure
Weight: approx. 180 g
Dimensions: 117 x 69 x 46 mm
IP Class: IP22
Reference to
standards:
EN 13544-1; EN 60601-1; EN 60601-2;
EN 60601-1-6; IEC 60601-1-11
Expected service life: 400 hours
The technical specifications may change without prior
notice.