KaVo MASTERmatic LUX M07 L, Инструкция по эксплуатации

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Instructions for use MASTERmatic LUX M07 L - 1.009.3610 MASTERmatic LUX M20 L - 1.009.3620 MASTERmatic LUX
M29 L - 1.009.3580
7 Reprocessing steps in accordance with ISO 17664 | 7.6 Packaging
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7.6 Packaging
Note
The sterilisation bag must be large enough for the handpiece so that the bag is not
stretched.
The quality and use of the sterilisation packaging must satisfy applicable standards
and be suitable for the sterilisation procedure!
▶ Weld each medical device individually in a sterilised item package!
7.7 Sterilisation
Sterilisation in a steam steriliser (autoclave) in accordance with EN
13060 / ISO 17665-1
CAUTION
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶ Before each sterilisation cycle, service the medical device with KaVo care prod‐
ucts.
CAUTION
Contact corrosion due to moisture.
Damage to product.
▶ Immediately remove the product from the steam steriliser after the sterilisation cy‐
cle!
The KaVo medical device has a maximum temperature resistance of up to 138 ℃
(280.4 °F).
Select a suitable procedure (depending on the available autoclave) from the following
sterilisation processes:
▪ Autoclave with three times pre-vacuum:
- at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4 °F)
▪ Autoclave 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.
7.8 Storage
▶ Reprocessed products should be stored protected from dust with minimum expo‐
sure to germs in a dry, dark and cool space.
Note
Comply with the expiry date of the sterilised items.