Registration number (WIID)Project No.TitleStatus
31723ISO 14155-1:2003Clinical investigation of medical devices for human subjects — Part 1: General requirementsAtcelts
18966ISO 10993-6:1994Biological evaluation of medical devices — Part 6: Tests for local effects after implantationAtcelts
18967ISO 10993-7:1995Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsAtcelts
90932ISO/CD TS 25364-3Analytical chemistry matters associated with ISO 10993-18 — Part 3: Instrumental and human requirements for evaluating organic medical device extractables and leachables via Non-Targeted Analysis (NTA)Izstrādē
41177ISO/WD 14155-2Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plansIzstrādē
64780ISO/WD TS 29741Biological evaluation of medical devices — Development of tolerable intake values for Di(2-ethylhexyl)phthalate (DEHP)Izstrādē
22696ISO 10993-4:1992/DAmd 1Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1Izstrādē
39204ISO 10993-12:2002/DAmd 1Biological evaluation of medical devices — Part 12: Sample preparation and reference materials — Amendment 1Izstrādē
31481ISO/DIS 10993-18Biological evaluation of medical devices — Part 18: Chemical characterization of materialsIzstrādē
71146ISO/NP TR 37137-1Cardiovascular biological evaluation of medical devices — Guidance for absorbable implants — Part 1: Title missingIzstrādē
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