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AAMI TIR56

Guidance for the development, validation and routine control of an ethylene oxide sterilization process utilizing flexible bag systems for the sterilization of medical devices

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Organization: AAMI
Publication Date: 1 January 2013
Status: active
Page Count: 39
scope:

This TIR includes information to be considered during the development, validation, and routine control of EO sterilization processes that are performed using gas diffusion within individually sealed flexible sterilization bags.

Document History

AAMI TIR56
January 1, 2013
Guidance for the development, validation and routine control of an ethylene oxide sterilization process utilizing flexible bag systems for the sterilization of medical devices
This TIR includes information to be considered during the development, validation, and routine control of EO sterilization processes that are performed using gas diffusion within individually sealed...
January 1, 2013
Guidance for the development, validation and routine control of an ethylene oxide sterilization process utilizing flexible bag systems for the sterilization of medical devices
This AAMI Technical Information Report (TIR) provides information to be considered during the development, validation, and routine control of EO sterilization processes that are performed using gas...

References

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