11
en
The external diameter of the opening is 22 mm, and is thus also compatible with all commonly
used 22 mm receptacle systems.
HUMIDOPHONE
®
PLUS O
2
- On the patient side, the plastic housing is equipped with a central
opening with 15 mm internal diameter, thereby allowing for connection to a 15 mm standard
connector.
The external diameter of the opening is 22 mm, and is thus also compatible with all commonly
used 22 mm receptacle systems.
An oxygen connecting piece fitted to the side of the housing (5 mm plug-in connection) enables
a connecting tube to be connected up, thereby allowing combination with an oxygen source.
8. APPLICATION
Check whether the packaging and the product are in a faultless condition.
Check the use-by or expiry date.
Do not use the product after this date.
Use with a 15 mm connector: mount the
HUMIDOPHONE
®
with the central 15 mm opening by
means of light pressure on the 15 mm standard connector of the tracheostomy tube ➊.
Use with a 22 mm connector: mount the
HUMIDOPHONE
®
by means of light pressure on the
housing ring of the tracheostomy tube ➋, until the housing snaps in audibly through the outer
fastening rim.
Remove the
HUMIDOPHONE
®
by holding the tracheostomy tube firmly with two fingers in or
-
der to extract the filter cassette by tugging lightly ➍/➎.
9. HYGIENE INSTRUCTIONS
The
HUMIDOPHONE
®
is a single-patient product and is intended for single use only.
They must not be cleaned or disinfected, as use of disinfectant can render the filter unusable.
In addition, bacterial or fungicidal colonisation of the filter material can lead to an increased
risk of infection.
Cleaning, disinfection or (re-)sterilisation as well as use longer than 24 hours can impair the
safety and function of the product and are therefore not permissible!
10. STORAGE
This product should be stored in a dry environment away from sunlight and/or heat.
11. SERVICE LIFE
The maximum period of use / wearing period is 24 hours ➎.
If necessary, the filter must be changed several times a day, for instance if the respiratory re
-
sistance is in danger of increasing due to accumulation of secretions.
12. DISPOSAL
The product must only be disposed of in accordance with the national regulations.
13. LEGAL NOTICES
The manufacturer Andreas Fahl Medizintechnik-Vertrieb GmbH will not accept any liability for
damages (in particular for functional deficiencies, injuries, infections, and/or other complica
-
tions or adverse events) caused by unauthorised product alterations, by repairs not performed
by the manufacturer or by improper handling, care (cleaning/disinfection) and/or storage of the
products in violation of the provisions of these instructions for use.
This applies – to the extent permitted by law – both to damages to the products themselves
caused thereby as well as to any consequential damages caused thereby.
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