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DILUMAT S® MA108201-C
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RECOMMENDATIONS
ASSOCIATED WITH BIOLOGICAL
CONTAMINATION RISKS
Purpose
To protect people involved with analysis systems, instruments
and all of their parts must be decontaminated before use. This
goal is based on the competence of biologists and the
recommendations of providers.
Methods

The biologist will decontaminate the device as specified in the
user guide within a timely manner and record the
decontamination in the maintenance log.

The biologist must identify the level of risk associated with
their work (HIV, mycobacteria, prions, etc.) and note it in the
maintenance log for those outside the laboratory.

It is recommended to protect the outside of the instrument
during transport (box, film, cover).
Process Application for Instruments
 For external actions involving the instruments (maintenance
technician, biomedical engineer, etc.)
 When repairing instruments at the user site before movement
by a carrier (returns, moves)
The declaration of decontamination must include:

The name of the material and its serial number

The individual performing the decontamination

The protocol used
It must be signed and dated.
References
Framework directive 89/391/CEE on implementing measures for
improving on-the-job health and safety for workers
Directive 90/679/CEE on protecting workers against risks
associated with on-the-job exposure to biological agents.
Law dated December 31, 1991 (Article L 230-1 to 5 of the Labor
Code)
Decree dated May 4, 1994 (Article R 231-60 to R 231-65.3 of the
Labor Code)
Decree dated July 16,2007 (J.O. dated August 4, 2007)