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.