Registration number (WIID)Project No.TitleStatus
75885FprEN ISO 10993-7Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2025)Izstrādē
75596EN ISO 10993-1:2025Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO/FDIS 10993-1:2025)Izstrādē
9483-Biological evaluation of medical devices - Methods of testing for degradation productsIzstrādē
77335prEN ISO 18969Clinical evaluation of medical devicesIzstrādē
77182FprEN ISO 14155Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025)Izstrādē
76054prEN ISO 8250Cleanliness of medical devices -- Process design and test methodsIzstrādē
40661prEN ISO 10993-7 revBiological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsIzstrādē
31980prEN ISO 10993-5Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Izstrādē
9485-Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residualsIzstrādē
40814prEN ISO 10993-5 revBiological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Izstrādē
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