ISO/TC 198
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 74152 | ISO 17664-2:2021 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices | Standarts spēkā |
| 43187 | ISO 17665-1:2006 | Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 62244 | ISO 18362:2016 | Manufacture of cell-based health care products — Control of microbial risks during processing | Standarts spēkā |
| 35047 | ISO 18472:2006 | Sterilization of health care products — Biological and chemical indicators — Test equipment | Atcelts |
| 66450 | ISO 18472:2018 | Sterilization of health care products — Biological and chemical indicators — Test equipment | Standarts spēkā |
| 39778 | ISO 20857:2010 | Sterilization of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilization process for medical devices | Standarts spēkā |
| 73214 | ISO 22441:2022 | Sterilization of health care products — Low temperature vaporized hydrogen peroxide — Requirements for the development, validation and routine control of a sterilization process for medical devices | Standarts spēkā |
| 51772 | ISO 25424:2009 | Sterilization of medical devices — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 70822 | ISO 25424:2018 | Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices | Standarts spēkā |
| 81821 | ISO 25424:2018/Amd 1:2022 | Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Standarts spēkā |
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