Magic Care Aliseo Plus, Инструкция по эксплуатации

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TROUBLESHOOTING
PROBLEM REMEDY
1. While pressing the handset button the
LED is not lit.
- When operating through mains sup-
ply make sure that the handset and the
power supply unit are properly plugged
in.
- When operating through a cigarette-
lighter socket (optional accessory),
check that the cord is properly plugged
in and the fuse is not burnt out.
2. In the case of poor nebulisation - Make sure that the drug is not too cold
– drug temperature should be close to
room temperature.
3. If the unit does not nebulise - Make sure the drug is not glycol-based
and always remember that the use of an
ultrasonic nebulizer is not recommend-
ed.
- Check that the nebulising chamber con-
tains medication.
- Make sure that quantity of medication is
between 4 and 8 ml max.
- Check that the medication is diluted suf-
ficiently with saline solution 0.9%.
- Make sure that the flow adjustment
knob is not in the “STOP” position.
- Check that the transparent cover (A6)
and the disk positioned below are clean.
4. If the appliance interrupts nebulisation
and the green LED flashes, this means
there is no more medication.
- Put some more medication into the tray
or proceed to clean.
5. Failure to clean the nebuliser from drug
deposits may endanger proper operation
of the unit.
- Carefully follow the instructions for
CLEANING, SANITIZATION AND DISIN-
FECTION.
Should the unit again fail to operate after following the above instructions, please con-
tact your local dealer or authorised after-sales centre.
NOTICE (ref. A Directive 2007/47/EC)
Flaem Nuova SpA has been manufacturing top-quality electro-medical appliances for the past 40 years
or more, using carefully selected and tested materials in compliance with the requirements of reference
directives and standards, with patient/user safety as number one priority. Because of this, we are able to
state that the use of the Flaem device and original accessories purchased by you does not involve any
risk whatsoever for the user’s health.
The specific tests conducted at accredited laboratories (as per UNI EN ISO 10993-17: 2004 rule
on Biological Assessment Part 17 Definition of allowable limits for leachable substances) actually
demonstrate that the BPA used is released in amounts much lower than the maximum allowed for the
safety threshold.