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
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...
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...