Drying
❯
Allow the device to air-dry.
The device must be completely dry before a
new hygienic protective cover is fitted.
10 Reprocessing the spacer
10.1 Risk analysis and categorisa-
tion
A risk analysis and categorisation of medical
products often used in dentistry must be per-
formed before their reprocessing by the operator.
Comply with all national directives, standards and
specifications such as e. g. the "Recommenda-
tions from the Commission for Hospital Hygiene
and Infection Prevention".
Accessories of the medical device are also sub-
ject to reprocessing.
Classification recommendation given intended
use of the product:
semi-critical B
Semi-critical medical product:
A medical product which comes into contact
with mucous membrane or pathologically
affected skin.
The operator is responsible for correct classifica-
tion of the medical products, defining the repro-
cessing steps and performing the reprocessing.
10.2 Reprocessing procedure in
accordance with EN ISO
17664
The reprocessing procedure after each patient
treatment is carried out according to the repro-
cessing procedure established by EN ISO 17664.
Usage
2109100026L02 1907V001
31
EN
Summary of Contents for VistaCam iX HD Smart
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