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This part of ISO 11137 specifies methods for determining the minimum dose needed to achieve a specified requirement for sterility and methods to substantiate the use of 25 kGy or 15 kGy as the sterilization dose to achieve a sterility assurance level, SAL, of 10-6. This part of ISO 11137 also specifies methods of sterilization dose audit used to demonstrate the continued effectiveness of the sterilization dose. This part of ISO 11137 defines product families for sterilization dose establishment and sterilization dose audit.
Author | ANSI/AAMI/ISO |
---|---|
Editor | AAMI |
Document type | Standard |
Format | File |
Confirmation date | 2013-07-10 |
ICS | 11.080.99 : Other standards related to sterilization and disinfection |
Replace | ANSI/AAMI/ISO 11137-2 (2012) |
Cross references | ISO 11137-2 (2013-06), IDT |
Year | 2013 |
Document history | ANSI/AAMI/ISO 11137-2 (2013) |
Country | USA |
Keyword | ANSI 11137;ANSI/AAMI/ISO 11137;11137;ANSI/AAMI/ISO 11137-2, third edition-2013 |