ISO/TC 198
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
55080 | ISO 11140-1:2014 | Sterilization of health care products — Chemical indicators — Part 1: General requirements | Standarts spēkā |
56137 | ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices | Standarts spēkā |
56650 | ISO 15883-7:2016 | Washer-disinfectors — Part 7: Requirements and tests for washer-disinfectors employing chemical disinfection for non-invasive, non-critical thermolabile medical devices and healthcare equipment | Atcelts |
59366 | ISO 11607-1:2006/Amd 1:2014 | Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1 | Atcelts |
59368 | ISO 11607-2:2006/Amd 1:2014 | Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1 | Atcelts |
59405 | ISO/AWI 17210 | Test method to demonstrate the suitability of a medical device simulator during steam sterilization — Medical device simulator testing | Izstrādē |
59475 | ISO 13408-1:2008/Amd 1:2013 | Aseptic processing of health care products — Part 1: General requirements — Amendment 1 | Atcelts |
59476 | ISO 13408-6:2005/Amd 1:2013 | Aseptic processing of health care products — Part 6: Isolator systems — Amendment 1 | Atcelts |
59843 | ISO 15883-1:2006/Amd 1:2014 | Washer-disinfectors — Part 1: General requirements, terms and definitions and tests — Amendment 1 | Atcelts |
60165 | ISO 11137-1:2006/Amd 1:2013 | Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Atcelts |
Displaying 121-130 of 206 results.