Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019)
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)
Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)
Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)
Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)
Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
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 devices (ISO 14937:2009)
Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018)
Information supplied by the manufacturer of medical devices
53,361 distinct reference strings indexed from official source snapshots accessed on 19 October 2026. Includes earlier editions. The index and publisher collections have different coverage. See sources and coverage.