6
• Turn on by pressing the on/o switch and start therapy;
• During the treatment session, the nebuliser cup can be rested on its own support;
• Carry out treatment preferably seated and in a comfortable position;
• When the aerosol jet becomes intermittent, interrupt the treatment for a few seconds to allow the suspended
drops of solution to fall on the nebuliser cup walls. Resume the treatment session, which will be nished when
no more nebulised solution is released from the nebuliser cup;
• Once the treatment session is completed, switch the device o by unplugging it, remove the accessory used
and clean the device and accessories according to the instructions in the Cleaning and Maintenance paragraph.
• The patient and operator are the same person. The steps that the patient/user can do safely are only those
specied in the paragraphs “Preparing and using the appliance,” “Cleaning and maintenance of the compressor,
nebuliser cup and accessories.” Warning! Do not service and/or repair the appliance while it is being used! Any
other maintenance/service activity/operation must be done solely by a PiC Service Centre.
COMPRESSOR CLEANING AND MAINTENANCE
Warning! Do not wet the device or put it into water or other liquids. For cleaning, use a clean, dry cloth only.
CLEANING AND MAINTENANCE OF THE NEBULISER CUP AND ACCESSORIES
Remove and detach all the nebuliser cup components and dip them in boiling water for about 5 minutes.
Rinse the accessories (mask, mouthpiece, fork and tube) under running water. Cold disinfect all parts that come in
contact with the patient using denatured alcohol. Carefully dry all accessories and the device before reassembling.
Store the device and the accessories in a cool, dry place, away from light and heat.
Never use benzene, thinners or other inflammable chemical substances for cleaning.
For increased hygienic safety, never use the same accessories on more than one patient. Purchase a dedicated kit
for each user (Aerosol Kit 02004990000000).
Clean and check that the condition of the accessories before and after use. Replace them if damaged.
CHECKING AND REPLACING FILTERS
Periodically check the condition of the lter. The lter was inserted to protect the compressor.
Correct lter maintenance prolongs the life of the aerosol. The frequency with which lter should be replaced
depends on the conditions in which the device is used. The lter is located in the upper part of the aerosol.
TO REPLACE THE FILTER:
• Remove the lter cover by lifting it up carefully, using a tool with a at blade;
• Remove the lter to be replaced from its seat;
• Carefully t the new lter;
• Reposition the lter cover by pushing it down fully in its seat, making sure that it cannot be removed without
the use of a tool.
TYPE OF DEFECT CAUSE SOLUTION
Scarce nebulisation Clogged nebuliser cup Remove and detach all the nebu-
liser cup components and clean
them as illustrated in this instruc-
tion manual.
Scarce nebulisation Clogged nebuliser cup If the issue persists after cleaning,
replace the nebuliser cup.
No nebulisation Nebuliser cup components not as-
sembled correctly
Disassemble and reassemble the
nebuliser cup; if the issue persists,
replace the nebuliser cup.
No nebulisation The compressor does not work Check that the power cord plug is
disconnected from the mains and
that the on/off switch is on. If the
issue persists, contact a PIC Servi-
ce Centre.
Slow nebulisation Drug too thick Dilute the drug as instructed by
the manufacturer.
TECHNICAL SPECIFICATIONS
Nominal voltage: 230 V~ Service life in storage conditions: 1 year
Absorbed current: 1A Frequency: 50 Hz
Maximum ow: 13.5 ± 2 l/min Fuse: T 1 H 250V, 5x20mm
Max pressure: 2.2 ± 0.6 atm Operational ow: 6 ± 1 l/min
Conditions for using the device: 20' ON - 40' OFF at 40 °C Operational pressure: 0.65 ± 0.2 atm
MMAD: < 3.7 μm Weight: 1.2 kg
Nebuliser cup capacity: 10 ml Max ; 2ml Min Breathable fraction: 65.7 % ± 3.4
Device service life: 1,000 cycles/treatments Noise level at 50 cm*: 68 dB
Service life of accessories: 1 year
* Data on noise levels were measured on a new device. Values may vary over time with use.
The information on the unit’s capabilities provided by the manufacturer in accordance with EN 13544-1 may not
apply to medicines provided in suspension form or those that are highly viscous.
EN 60601-1 Medical electrical equipment – Part 1: general requirements for safety
EN 60601-1-2 Medical electrical equipment – Part 1: General requirements for basic safety and essential
performance.
- Collateral standard: electromagnetic compatibility.
- Requirements and tests.
EN 13544-1 Respiratory therapy equipment – Part one: Nebulising systems and their components
This section contains information specic to product compliance with the EN 60601-1-2 standard. AirCube is a
medical electrical device that requires special precautions regarding electromagnetic compatibility and needs to
be installed and commissioned according to the electromagnetic information provided.
Mobile and portable RF communications equipment (mobile phones, transceivers, etc.) may affect the device.
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