KaVo 1.010.0287, Instructions For Use Manual

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Instructions for use PROPHYflex 4 Perio Kit – 1.011.9403 Refill PROPHYflex perio tip – 1.010.0287
6 Reprocessing steps in accordance with ISO 17664 | 6.5 Visual inspection and functional check
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6.5 Visual inspection and functional check
Note
Plug the adaptor with the PROPHYflex perio tip onto the PROPHYflex with an
empty powder container, and check it.
6.6 Care products and systems - Servicing
NOTICE
Improper care.
Malfunction or property damage.
▶ Do not service the PROPHYflex perio tip and adapter with oils or care spray.
6.7 Packaging
Note
The sterilisation bag must be large enough to accommodate the perio tip
without stretching the bag.
The quality and use of the sterilisation packaging must comply with applic-
able standards and be suitable for the sterilisation procedure!
▶ The medical device must be packed before sterilisation.
6.8 Sterilisation
Sterilisation in a steam steriliser (autoclave) in
accordance with EN 13060 / EN ISO 17665-1
NOTICE
Contact corrosion due to moisture.
Damage to product.
▶ Immediately remove the product from the steam steriliser after the steril-
isation cycle.
Note
Prior to attaching the powder container, all powder-conducting parts and air
channels must be absolutely dry. Screw together the powder container and
handpiece only while the parts are cold.
The KaVo medical device has a maximum temperature resistance up to 138 ℃
(280.4 °F).
Sterilisation parameters:
Select a suitable process from the following sterilisation processes (depending
on the available steriliser):
Steriliser 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)