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ISO 11140-1

Sterilization of health care products - Chemical indicators Part 1: General requirements

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Organization: ISO
Publication Date: 15 July 2005
Status: inactive
Page Count: 34
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

ISO 11140-1
November 1, 2014
Sterilization of health care products - Chemical indicators - Part 1: General requirements
This part of ISO 11140 specifies general requirements and test methods for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances, and...
ISO 11140-1
July 15, 2005
Sterilization of health care products - Chemical indicators Part 1: General requirements
A description is not available for this item.
ISO 11140-1
December 1, 1998
Sterilization of Health Care Products - Chemical Indicators - Part 1: General Requirements
A description is not available for this item.
ISO 11140-1
July 15, 1995
Sterilization of Health Care Products - Chemical Indicators - Part 1: General Requirements
A description is not available for this item.

References

This document is referenced by:
BS 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
Published by BSI on March 31, 2010
A description is not available for this item.
This document is referenced by:
ISO 20857 - Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2010
Inclusions This International Standard specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. NOTE Although the scope of...
This document is referenced by:
SN 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
Published by SNV on March 1, 2010
Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a...
This document is referenced by:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
This document is referenced by:
EN ISO 17665-1 - Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by CEN on August 1, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
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