Registration number (WIID)Project No.TitleStatus
86270ISO 15223-1:2021/Amd 1:2025Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements — Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specificStandarts spēkā
42343ISO 15223-2:2010Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validationStandarts spēkā
38421IEC 62304:2006Medical device software — Software life cycle processesStandarts spēkā
79173ISO 80369-7:2021Small-bore connectors for liquids and gases in healthcare applications — Part 7: Connectors for intravascular or hypodermic applicationsStandarts spēkā
65624IEC/TR 80002-3:2014Medical device software — Part 3: Process reference model of medical device software life cycle processes (IEC 62304)Standarts spēkā
69336ISO/TS 11633-1:2019Health informatics — Information security management for remote maintenance of medical devices and medical information systems — Part 1: Requirements and risk analysisStandarts spēkā
77326ISO 15223-1:2021Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirementsStandarts spēkā
50730ISO/DIS 80369-2Small bore connectors for liquids and gases in healthcare applications — Part 2: Connectors for breathing systems and driving gases applicationsStandarts spēkā
72042IEC 62366-1:2015/Cor 1:2016Medical devices — Part 1: Application of usability engineering to medical devices — Technical Corrigendum 1Standarts spēkā
54146IEC/TR 80002-1:2009Medical device software — Part 1: Guidance on the application of ISO 14971 to medical device softwareStandarts spēkā
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