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ISO 25424 FRENCH

Stérilisation des dispositifs médicaux - Formaldéhyde et vapeur à faible température - Exigences pour le développement, la validation et le contrôle de routine d'un procédé de stérilisation pour dispositifs médicaux

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Organization: ISO
Publication Date: 1 September 2009
Status: inactive
Page Count: 50
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

ISO 25424 FRENCH
October 1, 2018
Stérilisation des produits de santé - Formaldéhyde et vapeur à faible température - Exigences pour le développement, la validation et le contrôle de routine d'un procédé de stérilisation pour dispositifs médicaux
A description is not available for this item.
ISO 25424 FRENCH
September 1, 2009
Stérilisation des dispositifs médicaux - Formaldéhyde et vapeur à faible température - Exigences pour le développement, la validation et le contrôle de routine d'un procédé de stérilisation pour dispositifs médicaux
A description is not available for this item.

References

This document references:
AAMI RD47 - Reprocessing of hemodialyzers
Published by AAMI on January 1, 2020
This recommended practice describes the essential elements of good practice for reprocessing hemodialyzers to help ensure device safety and effectiveness. These practices embrace considerations of...
This document references:
EN 14180 - Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing
Published by CEN on May 1, 2014
A description is not available for this item.
This document references:
EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by CEN on October 1, 2001
This European Standard specifies the requirements for a terminally-sterilized medical device to be designated "STERILE". Part 2 of this European Standard specifies the requirements for an aseptically...
This document references:
EN 867-5 - Non-Biological Systems for Use in Sterilizers - Part 5: Specification for Indicator Systems and Process Challenge Devices for Use in Performance Testing for Small Sterilizers Type B and Type S
Published by CEN on August 1, 2001
A description is not available for this item.
This document references:
EN 868-1 - Packaging Materials and Systems for Medical Devices Which Are to Be Sterilized - Part 1: General Requirements and Test Methods
Published by CEN on February 1, 1997
A description is not available for this item.
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