ISO/TC 198
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31458 | ISO/DIS 11135 | Sterilization of health care products — Ethylene oxide — Requirements for development, validation and routine control of a sterilization process for medical devices | Izstrādē |
| 54072 | ISO/NP 11140-6 | Sterilization of health care products — Chemical indicators — Part 6: Class 2 indicators and process challenge devices for use in performance testing of steam sterilizers | Izstrādē |
| 73392 | ISO 11138-5:2017/NP Amd 1 | Sterilization of health care products — Biological indicators — Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes — Amendment 1: Annex C: Alternative method for determining the D-value of LTSF SCBI | Izstrādē |
| 29428 | ISO/WD 15883 | Sterilization of health care products — Washer disinfectors — Performance requirements and tests methods | Izstrādē |
| 54998 | ISO/NP 11737-4 | Sterilization of medical devices — Microbiological methods — Part 4: Sterility test on sterile medical devices | Izstrādē |
| 65304 | ISO/DTS 19572 | Sterilization of health care products — Guidance on the application of ISO14937 to the sterilization of medical devices using Ethylene Oxide in a flexible sterilization chamber | Izstrādē |
| 30060 | ISO/CD 13408-4 | Aseptic processing of health care products — Part 4: Cleaning in place | Izstrādē |
| 31454 | ISO/DIS 15883-3.2 | Washer-disinfectors — Part 3: Requirements and tests for washer-disinfectors employing thermal disinfection for human waste containers | Izstrādē |
| 86186 | ISO/DTS 17664-3 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 3: Guidance on the designation of a reusable medical device to a cleaning classification | Izstrādē |
| 93090 | ISO 14937:2009/WD Amd 1 | 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 — Amendment 1 | Izstrādē |
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