Full Description

This collection of 37 documents was updated in late 2010 to include nine new/ revised standards. It features new guidance for ethylene oxide, radiation, biological indicators, validation and control of a sterilization process, and test methodologies.

Contents14937 Sterilization of health care products -General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices14161 Sterilization of health care products -Biological indicators -Guidance for the selection, use, and interpretation of results15882 Sterilization of health care products -Chemical indicators -Guidance for selection, use and interpretation of results11737-1 Sterilization of medical devices -Microbiological methods -Part 1: Determination of a population of microorganisms on products11737-2 Sterilization of medical devices -Microbiological methods -Part 2: Tests of sterility performed in the validation of a sterilization processST72 Bacterial endotoxin-Test methodologies, routine monitoring and alternatives to batch testing17665-1 Sterilization of health care products -Moist heat -Part 1 Requirements for the development, validation and routine control of a sterilization process for medical devices17665-2 Sterilization of health care products -Moist heat -Part 2: Guidance on the application of ANSI/AAMI/ISO 17665-111135-1 Sterilization of health care products -Ethylene oxide -Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devicesTIR11135-2 Sterilization of health care products -Ethylene oxide -Part 2: Guidance on the application of ANSI/AAMI/ISO 11135-1TIR14 Contract sterilization using ethylene oxideTIR15 Physical aspects of ethylene oxide sterilizationTIR16 Microbiological aspects of ethylene oxide sterilizationTIR28 Product adoption and process equivalence for ethylene oxide sterilization10993-7 Biological evaluation of medical devices -Part 7: Ethylene oxide sterilization residuals11137-1 Sterilization of health care products -Radiation -Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices11137-2 Sterilization of health care products -Radiation -Part 2: Establishing the sterilization dose11137-3 Sterilization of health care products -Radiation -Part 3: Guidance on dosimetric aspectsTIR33 Sterilization of health care products -Radiation sterilization -Substantiation of a selected sterilization dose -Method VDmaxTIR35 Sterilization of health care products -Radiation sterilization -Alternative sampling plans for verification dose experiments and sterilization dose auditsTIR37 Sterilization of health care products --Radiation --Guidance on sterilization of human tissue-based products TIR40 Sterilization of health care products --Radiation --Guidance on dose setting utilizing a Modified Method 2TIR17 Compatibility of materials subject to sterilization14160 Sterilization of single-use medical devices incorporating materials of animal origin -Validation and routine control of sterilization by liquid chemical sterilantsST63 Sterilization of health care products --Requirements for the development, validation and routine control of an industrial sterilization process for medical devices--Dry heatTIR11139 Sterilization of health care products -VocabularyST67 Sterilization of medical devices-Requirements for products labeled "STERILE"11607-1 Packaging for terminally sterilized medical devices -Part 1: Requirements for materials, sterile barrier systems and packaging11607-2 Packaging for terminally sterilized medical devices -Part 2: Validation requirements for forming, sealing and assembly processesTIR22 Guidance for ANSI/AAMI/ISO 11607, Packaging for terminally sterilized medical devices -Part 1 and Part 2:200613408-1 Aseptic processing of health care products -Part 1: General requirements13408-2 ANSI/AAMI/ISO 13408-2:2003, Aseptic processing of health care products -Part 2: Filtration13408-3 ANSI/AAMI/ISO 13408-3:2006, Aseptic processing of health care products -Part 3: Lyophilization13408-4 ANSI/AAMI/ISO 13408-4:2005, Aseptic processing of health care products -Part 4: Clean-in-place technologies13408-5 ANSI/AAMI/ISO 13408-5:2006, Aseptic processing of health care products -Part 5: Sterilization in place13408-6 ANSI/AAMI/ISO 13408-6:2005, Aseptic processing of health care products -Part 6: Isolator systems

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Part of: AAMI STBK10-S/STBKCD