ISO/TC 198
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
66566 | ISO/TS 19930:2017 | Guidance on aspects of a risk-based approach to assuring sterility of terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a sterility assurance level of 10-6 | Atcelts |
62952 | ISO 17664:2017 | Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices | Atcelts |
53573 | ISO/TS 11135-2:2008/Cor 1:2009 | Sterilization of health care products — Ethylene oxide — Part 2: Guidance on the application of ISO 11135-1 — Technical Corrigendum 1 | Atcelts |
41175 | ISO/TS 15883-5:2005 | Washer-disinfectors — Part 5: Test soils and methods for demonstrating cleaning efficacy | Atcelts |
35047 | ISO 18472:2006 | Sterilization of health care products — Biological and chemical indicators — Test equipment | Atcelts |
43350 | ISO 14161:2009 | Sterilization of health care products — Biological indicators — Guidance for the selection, use and interpretation of results | Atcelts |
53572 | ISO 11137-2:2006/Cor 1:2009 | Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose — Technical Corrigendum 1 | Atcelts |
22967 | ISO 14160:1998 | Sterilization of single-use medical devices incorporating materials of animal origin — Validation and routine control of sterilization by liquid chemical sterilants | Atcelts |
46116 | ISO 11737-1:2006/Cor 1:2007 | Sterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on products — Technical Corrigendum 1 | Atcelts |
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 |
Displaying 91-100 of 206 results.