Abstract
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: WithdrawnPublication date: 2009-11Stage: Withdrawal of International Standard [95.99]
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Edition: 2Number of pages: 16
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Technical Committee :ISO/TC 198
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Life cycle
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Previously
WithdrawnISO 11737-2:1998
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Now
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Revised by
PublishedISO 11737-2:2019