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ISO 11737-2:2009

Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process

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Publication date: 2009-11-15
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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.
Document identifier
ISO 11737-2:2009
Title
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
ISO Category
TC 198: Sterilization of health care products
Publication date
2009-11-15
Status
Effective
International Relationship
BS EN ISO 11737-2:2009 * AAMI/ISO 11737-2:2009/(R)2014 * DIN EN ISO 11737-2
Cross references
Latest version
ISO 11737-2:2009
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
Document identifier ISO 11737-2:2009
Publication date 2009-11-15
Classification 07.100.10. Medical microbiology
11.080.01. Sterilization and disinfection in general
Status Effective
*
History of version
ISO 11737-2:2009 * ISO 11737-2:1998
Keywords
Classification
07.100.10. Medical microbiology
11.080.01. Sterilization and disinfection in general
Pages
Price Contact

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