Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1: Applicability of allowable limits for neonates and infants
Edition 2019-12

Sterilization of health care products - Biological indicators - Part 8: Method for validation of a reduced incubation time for a biological indicator (ISO 11138-8:2021)
Edition 2021-08

Sterilization of health care products - Biological indicators - Part 7: Guidance for the selection, use and interpretation of results (ISO 11138-7:2019)
Edition 2019-11

Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018)
Edition 2018-07

Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2017)
Edition 2017-06

Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017)
Edition 2017-11

Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2014)
Edition 2015-01

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
Edition 2015-11

Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)
Edition 2011-09

Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices; Corrigendum AC
Edition 2006-12