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.
Текущий статус : WithdrawnДата публикации : 2009-11
Версия : 2
Технический комитет:Sterilization of health care products