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AAMI - TIR28

PRODUCT ADOPTION AND PROCESS EQUIVALENCY FOR ETHYLENE OXIDE STERILIZATION

inactive
Organization: AAMI
Publication Date: 1 January 2001
Status: inactive
Page Count: 22

Document History

AAMI TIR28
January 1, 2016
Product adoption and process equivalence for ethylene oxide sterilization
This TIR addresses medical devices that are processed by ethylene oxide (EO) sterilization using conventional or parametric product release. The document applies to the following situations for the...
TIR28
January 1, 2016
Product adoption and process equivalence for ethylene oxide sterilization
This TIR addresses medical devices that are processed by ethylene oxide (EO) sterilization using conventional or parametric product release. The document applies to the following situations for the...
TIR28
January 1, 2009
Product adoption and process equivalence for ethylene oxide sterilization
This TIR addresses medical devices that are processed by ethylene oxide (EO) sterilization using conventional or parametric product release. The document applies to the following situations for the...
TIR28
January 1, 2009
Product adoption and process equivalence for ethylene oxide sterilization
This TIR addresses medical devices that are processed by ethylene oxide (EO) sterilization using conventional or parametric product release. The document applies to the following situations for the...
TIR28
January 1, 2001
PRODUCT ADOPTION AND PROCESS EQUIVALENCY FOR ETHYLENE OXIDE STERILIZATION
A description is not available for this item.

References

Refer to:
ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on July 15, 2014
Inclusions This International Standard specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial...
Refer to:
AAMI 11135 - Sterilization of health care products - Ethylene oxide - Requirements for development, validation and routine control of a sterilization process for medical devices
Published by AAMI on January 1, 2014
Inclusions This International Standard specifies requirements for the development, validation, and routine control of an ethylene oxide sterilization process for medical devices in both the...
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