Care instructions KaVo uniQa
2 Reprocessing steps in accordance with ISO 17664 | 2.7 Reprocessing the three-function and multifunctional
handpiece
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NOTE
Please comply with the instructions for use of the washer disinfector.
4
In order not to affect the KaVo medical device, make sure that the product
is dry on the inside and outside after completion of the cycle.
4
Remove any residual liquids through subsequent sterilisation.
2.7.5 Care products and systems - Servicing
CAUTION
Improper care.
Malfunction or property damage.
4
Do not service the medical device with oil or maintenance spray.
4
Apply KaVo silicone grease (
Mat. no. 1.000.6403
) to the O-rings of the
joint between the gripping sleeve and cannula for servicing. Use cotton buds
for this purpose.
2.7.6 Packaging
NOTE
The sterile goods package must be large enough to accommodate the product
without stretching the packaging. The quality and use of the packaging of the
items to be sterilised must meet the applicable standards and be appropriate
for the sterilisation process!
4
Seal medical devices (cannula and gripping sleeve) separately in sterile
good packaging.
2.7.7 Sterilisation in a steam steriliser (autoclave) in
accordance with EN 13060 / EN ISO 17665-1
CAUTION
Contact corrosion due to moisture.
Damage to product.
4
Immediately remove the product from the steam steriliser after the steril-
isation cycle.
CAUTION
Damage caused by over-heating.
Damage to the gripping sleeve.
4
Immediately remove the parts from the steriliser after the sterilisation cycle
is completed.
The medical device has a max. temperature resistance of up to 138
o
C (280.4
o
F).
4
Sterilisation with a triple pre-vacuum:
- at least 3 minutes at 134 °C -1 °C/ +4 °C (273 °F -1.6 °F/ +7.4 °F)
4
Use according to the manufacturer's Instructions for Use.
2.7.8 Storage
Reprocessed products must be stored appropriately protected from dust in a
dry, dark and cool space with a low germ level.
NOTE
Comply with the expiry date of the sterilised items.
Summary of Contents for uniQa
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