Registration number (WIID)Project No.TitleStatus
66566ISO/TS 19930:2017Guidance 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 10-6Atcelts
62952ISO 17664:2017Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devicesAtcelts
53573ISO/TS 11135-2:2008/Cor 1:2009Sterilization of health care products — Ethylene oxide — Part 2: Guidance on the application of ISO 11135-1 — Technical Corrigendum 1Atcelts
41175ISO/TS 15883-5:2005Washer-disinfectors — Part 5: Test soils and methods for demonstrating cleaning efficacyAtcelts
35047ISO 18472:2006Sterilization of health care products — Biological and chemical indicators — Test equipmentAtcelts
43350ISO 14161:2009Sterilization of health care products — Biological indicators — Guidance for the selection, use and interpretation of resultsAtcelts
53572ISO 11137-2:2006/Cor 1:2009Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose — Technical Corrigendum 1Atcelts
22967ISO 14160:1998Sterilization of single-use medical devices incorporating materials of animal origin — Validation and routine control of sterilization by liquid chemical sterilantsAtcelts
46116ISO 11737-1:2006/Cor 1:2007Sterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on products — Technical Corrigendum 1Atcelts
51772ISO 25424:2009Sterilization of medical devices — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devicesAtcelts
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