Instructions for use PROPHYflex 3 - 2018 for Sirona connection - 1.006.9920, - 1.006.9927
7 Reprocessing steps in accordance with ISO 17664 | 7.5 Packaging
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7.5 Packaging
Note
The sterilisation bag must be large enough for the instrument so that the bag is not
stretched.
The quality and use of the sterilisation packaging must comply with applicable
standards and be suitable for the sterilisation procedure!
▶ Weld each medical device individually in a sterilised item package!
7.6 Sterilisation
Sterilisation in a steam steriliser (autoclave) in accordance with EN
13060 / ISO 17665-1
NOTICE
Contact corrosion due to moisture.
Damage to product.
▶ Immediately remove the product from the steam steriliser after the sterilisation
cycle.
Note
Prior to attaching the powder container, all powder-conducting parts and air chan-
nels must be absolutely dry. Screw together the powder container and handpiece
only in the cold state.
▶ Unscrew the powder container anticlockwise and drain and clean it before each
thermal disinfection or sterilisation.
▶ Do not screw the powder container back on before thermal disinfection or sterilisa-
tion.
▶ Likewise, clean off any powder residue on the PROPHYflex, especially the can-
nula, tubes and P-nozzle.
The KaVo medical device has a maximum temperature resistance up to 138 ℃
(280.4 °F).
Select a suitable procedure (depending on the available autoclave) from the following
sterilisation processes:
▪ Autoclave with triple pre-vacuum:
- at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
▪ Steriliser using the gravity method:
- at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
▶ Use according to the manufacturer's Instructions for Use.
7.7 Storage
▶ Reprocessed products should be stored protected from dust with minimum expos-
ure to germs in a dry, dark and cool place.
▶ Comply with the expiry date of the sterilised items.
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