Packaging; Sterilisation; Storage - KaVo DIAGNOcam Vision Full HD Instructions For Use Manual

7 Reprocessing steps in accordance with ISO 17664 | 7.7 Packaging

7.7 Packaging

Note
The sterile goods package must be large enough for the product so that the
packaging is not stretched.
The quality and use of the packaging of the items to be sterilised must satisfy
the applicable standards and be appropriate for the sterilisation process!
▶ The medical device must be packed before sterilisation.

7.8 Sterilisation

Sterilisation in a steam steriliser (autoclave) in
accordance with EN 13060 / EN ISO 17665-1
Damage to product.
Immediately remove the product from the steam steriliser after the sterilisation
cycle.
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)
▪ at least 60 minutes at 121 °C -1 °C / +4 °C (250 °F -1.6 °F / +7.4 °F)
▶ Use according to the manufacturer's Instructions for Use.

7.9 Storage

Prepared products must be stored appropriately in a dry, dark, cool room such
that they are protected from germs (as far as possible) and dust.
Note
Comply with the expiry date of the sterilised items.
Instructions for use DIAGNOcam Vision Full HD
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