Pari VORTEX Tracheo Mode D'emploi page 38

The frequency and duration of use is determined by profes-
sional medical staff according to the individual needs of the pa-
tient.
1.2 Indication
For treatment of diseases of the lower airways in combination
with a metered dose inhaler for use by tracheotomised pa-
tients.
1.3 Contraindications
There are no contraindications known to PARI GmbH.
1.4 Labelling
The following symbols can be found on the product and/or the
packaging:
Medical device
Legal manufacturer
Date of manufacture
This product conforms to the EU Medical Device
Regulation 2017/745.
Consult instructions for use
Item no.
Production batch number, lot number
Unique Device Identifier (UDI)
VORTEX
VORTEX tracheostomy adapter
– 6 –