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DIN EN ISO 14937

Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009); German version EN ISO 14937:2009

active, Most Current
Organization: DIN
Publication Date: 1 March 2010
Status: active
Page Count: 54
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

DIN EN ISO 14937
March 1, 2010
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009); German version EN ISO 14937:2009
A description is not available for this item.
DIN EN ISO 14937
January 1, 2008
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process
A description is not available for this item.
DIN EN ISO 14937 Berichtigung 1
June 1, 2005
Sterilization of health care products - General criteria for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000); Corrigendum to DIN EN ISO 14937:2001-05; German version EN ISO 14937:2000/AC:2005
A description is not available for this item.
DIN EN ISO 14937
May 1, 2001
Sterilization of health care products - General criteria for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000); German version EN ISO 14937:2000
A description is not available for this item.
DIN EN ISO 14937
June 1, 1999
Sterilization of health care products - General criteria for characterization of a sterilizing agent development, validation and routine control of a sterilizing process (ISO/DIS 14937:1999); German version prEN ISO 14937:1999
A description is not available for this item.

References

This document is referenced by:
DIN EN 1422 - Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods; German version EN 1422:2014
Published by DIN on August 1, 2014
Diese Europäische Norm legt die Anforderungen und entsprechenden Prüfverfahren für automatisch gesteuerte Sterilisatoren fest, die Ethylenoxid (EO) entweder als reines Gas oder als Gas im Gemisch mit...
This document is referenced by:
DIN EN ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018); German version EN ISO 11135:2014 + A1:2019
Published by DIN on April 1, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 11607-1 - Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019); German version EN ISO 11607-1:2020
Published by DIN on May 1, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)
Published by DIN on April 1, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 80601-2-69 - Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014); German version EN ISO 80601-2-69:2014
Published by DIN on December 1, 2014
IEC 60601-1:2005+Änderung 1:2012, 1.1 wird ersetzt durch: Diese besondere Norm legt Anforderungen an die BASISSICHERHEIT und die WESENTLICHEN LEISTUNGSMERKMALE eines SAUERSTOFF-KONZENTRATORS zusammen...
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