This standard was last reviewed and confirmed in 2015. Therefore this version remains current.
Abstract Preview
ISO 11737-2:2009 specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent reduced relative to that anticipated to be used in routine sterilization processing. These tests are intended to be performed when defining, validating or maintaining a sterilization process.
General information
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Status : PublishedPublication date : 2009-11
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Edition : 2Number of pages : 16
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- ICS :
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Medical microbiology
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Sterilization and disinfection in general
Buy this standard
| Format | Language | |
|---|---|---|
| Paper |
- CHF88
Life cycle
A standard is reviewed every 5 years
Revisions / Corrigenda
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Previously
ISO 11737-2:1998
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Now under review
ISO 11737-2:2009 -
Will be replaced by
ISO/FDIS 11737-2
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