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.
Revises
ISO 11737-2:1998
WITHDRAWN
ISO 11737-2:2009
95.99
Withdrawal of Standard
Dec 2, 2019
PUBLISHED
ISO 11737-2:2019
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