ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67943 | ISO 20417:2021 | Medical devices — Information to be supplied by the manufacturer | Standarts spēkā |
| 67942 | ISO/TR 20416:2020 | Medical devices — Post-market surveillance for manufacturers | Standarts spēkā |
| 67941 | ISO/DIS 15223-1 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements | Izstrādē |
| 67284 | ISO 18250-1:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methods | Standarts spēkā |
| 65684 | ISO 18250-8:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 8: Citrate-based anticoagulant solution for apheresis applications | Standarts spēkā |
| 65624 | IEC/TR 80002-3:2014 | Medical device software — Part 3: Process reference model of medical device software life cycle processes (IEC 62304) | Standarts spēkā |
| 64686 | IEC 62304:2006/Amd 1:2015 | Medical device software — Software life cycle processes — Amendment 1 | Standarts spēkā |
| 64419 | ISO 80369-1:2018 | Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements | Standarts spēkā |
| 63940 | ISO 16142-2:2017 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards | Atcelts |
| 63939 | ISO 16142-1:2016 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards | Atcelts |
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