ISO/TC 198
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 19542 | ISO 11607:1997 | Packaging for terminally sterilized medical devices | Atcelts |
| 38712 | ISO 11607-1:2006 | Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems | Atcelts |
| 38546 | ISO 14937:2000/Cor 1:2003 | 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 — Technical Corrigendum 1 | Atcelts |
| 19156 | ISO 11137:1995 | Sterilization of health care products — Requirements for validation and routine control — Radiation sterilization | Atcelts |
| 25989 | ISO 14937:2000 | 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 | Atcelts |
| 33765 | ISO 11140-4:2001 | Sterilization of health care products — Chemical indicators — Part 4: Class 2 indicators for steam penetration test packs | Atcelts |
| 22270 | ISO 13683:1997 | Sterilization of health care products — Requirements for validation and routine control of moist heat sterilization in health care facilities | Atcelts |
| 33964 | ISO 11737-3:2004 | Sterilization of medical devices — Microbiological methods — Part 3: Guidance on evaluation and interpretation of bioburden data | Atcelts |
| 20530 | ISO 11138-2:1994 | Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization | Atcelts |
| 44956 | ISO 14160:2011 | Sterilization 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 devices | Atcelts |
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