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ISO 11140-1:1995WithdrawnSterilization of health care products — Chemical indicators — Part 1: General requirementsISO 11737-2:2009WithdrawnSterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization processISO 11737-1:2006WithdrawnSterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on productsISO 11737-3:2004WithdrawnSterilization of medical devices — Microbiological methods — Part 3: Guidance on evaluation and interpretation of bioburden dataISO 11737-2:1998WithdrawnSterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the validation of a sterilization processISO 11737-1:1995WithdrawnSterilization of medical devices — Microbiological methods — Part 1: Estimation of population of microorganisms on productsISO/TS 13004:2013WithdrawnSterilization of health care products — Radiation — Substantiation of selected sterilization dose: Method VDmaxSDISO 13408-1:2008WithdrawnAseptic processing of health care products — Part 1: General requirementsISO 13408-6:2005WithdrawnAseptic processing of health care products — Part 6: Isolator systemsISO 13408-2:2003WithdrawnAseptic processing of health care products — Part 2: FiltrationISO 13408-1:1998WithdrawnAseptic processing of health care products — Part 1: General requirementsISO/TS 13409:2002WithdrawnSterilization of health care products — Radiation sterilization — Substantiation of 25 kGy as a sterilization dose for small or infrequent production batchesISO/TR 13409:1996WithdrawnSterilization of health care products — Radiation sterilization — Substantiation of 25 kGy as a sterilization dose for small or infrequent production batchesISO 13683:1997WithdrawnSterilization of health care products — Requirements for validation and routine control of moist heat sterilization in health care facilitiesISO 14160:2011WithdrawnSterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devicesISO 14160:1998WithdrawnSterilization of single-use medical devices incorporating materials of animal origin — Validation and routine control of sterilization by liquid chemical sterilantsISO 14161:2009WithdrawnSterilization of health care products — Biological indicators — Guidance for the selection, use and interpretation of resultsISO 14161:2000WithdrawnSterilization of health care products — Biological indicators — Guidance for the selection, use and interpretation of resultsISO 14937:2000WithdrawnSterilization 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 devicesISO/TS 15843:2000WithdrawnSterilization of health care products — Radiation sterilization — Product families and sampling plans for verification dose experiments and sterilization dose audits, and frequency of sterilization dose auditsISO/TR 15844:1998WithdrawnSterilization of health care products — Radiation sterilization — Selection of sterilization dose for a single production batchISO 15882:2003WithdrawnSterilization of health care products — Chemical indicators — Guidance for selection, use and interpretation of resultsISO 17664:2017WithdrawnProcessing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devicesISO 17664:2004WithdrawnSterilization of medical devices — Information to be provided by the manufacturer for the processing of resterilizable medical devicesISO/TS 17665-3:2013WithdrawnSterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization