Validation Test; On Site Validation Test; Periodical Validation Test; Routine Test - NSK iCare+ Mode D'emploi

3.3 Validation test

3.3.1. On site validation test

This test must be performed prior to first start-up. It consists of a series of tests in order to validate that the
functioning parameters are well respected after the installation of iCare+.

3.3.2. Periodical validation test

We recommend to perform this periodical validation test every year, in order to validate that the performance of
iCare+ is still optimum.

3.3.3. Routine test

A protein residual value determination using real contaminated instruments is part of the validation (chapter 3.3.1).
NSK recommends a periodic, quarterly, protein residual value determination outside the revalidation cycles.
The procedure is as follows:
- Attaching instruments from the practice circle after previous preparation in iCare+
(See the instructions for use chapter 12)
- Start the processing cycle
- Stop the processing cycle after the cleaning step has been completed and remove the instruments
Prior to the protein determination to be carried out according to the manufacturer, ensure that all fluids present in
the instrument and on the instrument are completely removed (using compressed air and using a suitable adapter)
in order to achieve a correct result. It is important to ensure that no cross-contamination occurs (e.g. by replacing
the protection gloves for each instrument, etc.)
Afterwards, the instrument has to be completely reprocessed again in iCare +.
iCare+ User Manual V11.4 • 09/2017 p. 18