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
52517ISO/TS 16775:2014Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2Atcelts
22967ISO 14160:1998Sterilization of single-use medical devices incorporating materials of animal origin — Validation and routine control of sterilization by liquid chemical sterilantsAtcelts
53572ISO 11137-2:2006/Cor 1:2009Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose — Technical Corrigendum 1Atcelts
60165ISO 11137-1:2006/Amd 1:2013Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 1Atcelts
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
33955ISO 11137-3:2006Sterilization of health care products — Radiation — Part 3: Guidance on dosimetric aspectsAtcelts
33956ISO 11138-1:2006Sterilization of health care products — Biological indicators — Part 1: General requirementsAtcelts
41078ISO 15883-3:2006Washer-disinfectors — Part 3: Requirements and tests for washer-disinfectors employing thermal disinfection for human waste containersAtcelts
19659ISO 11737-1:1995Sterilization of medical devices Microbiological methodsAtcelts
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