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AAMI - 11135 ERTA

Medical devices – Validation and routine control of ethylene oxide sterilization

inactive
Organization: AAMI
Publication Date: 6 April 2005
Status: inactive
Page Count: 1

Document History

January 1, 2014
Sterilization of health care products - Ethylene oxide - Requirements for development, validation and routine control of a sterilization process for medical devices
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...
11135 ERTA
April 6, 2005
Medical devices – Validation and routine control of ethylene oxide sterilization
A description is not available for this item.
January 1, 1994
Medical devices - Validation and routine control of ethylene oxide sterilization
A description is not available for this item.

References

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