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ISO 11140-3

Sterilization of health care products — Chemical indicators — Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test TECHNICAL CORRIGENDUM 1

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Organization: ISO
Publication Date: 1 November 2007
Status: active
Page Count: 28
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

ISO 11140-3
November 1, 2007
Sterilization of health care products — Chemical indicators — Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test TECHNICAL CORRIGENDUM 1
A description is not available for this item.
ISO 11140-3
March 15, 2007
Sterilization of health care products — Chemical indicators — Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test
A description is not available for this item.
ISO 11140-3
September 1, 2000
Sterilization of Health Care Products - Chemical Indicators - Part 3: Class 2 Indicators for Steam Penetration Test Sheets
A description is not available for this item.

References

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 13408-5 - Aseptic processing of health care products - Part 5: Sterilization in place
Published by CEN on June 1, 2011
This part of ISO 13408 specifies the general requirements for sterilization in place (SIP) applied to product contact surfaces of the equipment used in the manufacture of sterile health care products...
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...
This document is referenced by:
AAMI 13408-5 - Aseptic processing of health care products - Part 5: Sterilization in place
Published by AAMI on January 1, 2006
This part of ISO 13408 specifies the general requirements for sterilization in place (SIP) applied to product contact surfaces of the equipment used in the manufacture of sterile health care products...
This document is referenced by:
JIS T 11140-1 - Sterilization of health care products - Chemical indicators - Part 1: General requirements
Published by JSA on March 1, 2013
A description is not available for this item.
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