Reprocessing Of The Assistant Element; Preparing The Handpiece Holder - KaVo ESTETICA E30 Care Instructions

2 Reprocessing methods according to DIN EN ISO 17664 | 2.5 Reprocessing of the assistant element
Note
The use of hot-air sterilisation and radio-sterilisation is not permissible
(causes destruction of the products). KaVo shall not be held responsible if
non-permissible procedures such as ethylene oxide, formaldehyde, and low
temperature plasma sterilisation are used.
Note
Only cleaned and disinfected products may be sterilised.
Note
Please comply with the current local regulations governing the re-use and
disposal of equipment.
▶ Place the cleaned and disinfected tips, endo files, file holders, endo
wrenches and torque wrenches separately in sterilisation packages (e.g.
KaVo STERIclave bags Mat. no. 0.411.9912) and weld them to be sealed
or sterilise them in a sterilisation cassette (e.g. KaVo sterilisation cassette
Mat. no. 0.411.9101).
Sterilisation container requirements:
▪ EN 868 and ISO 11607
▪ Resistant up to 138
▪ Regular servicing
The requirements also apply to double disposable sterilisation packages.
Permissible sterilisation apparatus:
▪ Sterilisation apparatus with validated cycle parameters
▪ Sterilisation apparatus with non-validated cycle parameter which comply
with DIN EN ISO 14161:2000
Permissible procedures:
Procedures
Fractionated pre-vacuum
Steam sterilisation apparatus
(AAMI TIR no. 12, DIN EN ISO 14161,
DIN EN ISO 17665)
(DQ, IQ, OQ and PQ)
Storage
▶ Reprocessed products should be stored protected from dust with minimum
exposure to germs in a dry, dark and cool place.
▶ Comply with the expiry date of the sterilised items.

2.5 Reprocessing of the assistant element

2.5.1 Preparing the handpiece holder

Note
The handpiece holder can be removed.
o
C with appropriate permeability for steam
Time /Temperature
3 to 20 minutes at 132 °C/ 134 °C
o
138
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Care instructions ESTETICA E30
C