ISO/TC 198
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
86186 | ISO/AWI TS 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 |
90413 | ISO/AWI 25442 | Sterilization of health care products — Test procedure for Measurement of temperature, pressure, and humidity in equipment | Izstrādē |
89497 | ISO/AWI 25224 | Sterilization of health care products — Sampling and culturing for reusable, thermolabile flexible endoscopes | Izstrādē |
59405 | ISO/AWI 17210 | Test method to demonstrate the suitability of a medical device simulator during steam sterilization — Medical device simulator testing | Izstrādē |
90093 | ISO/AWI 11137-2 | Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose | Izstrādē |
81244 | ISO 25424:2018/CD Amd 1 | 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 | Izstrādē |
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 |
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 |
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 |
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 |
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