ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38421 | IEC 62304:2006 | Medical device software — Software life cycle processes | Standarts spēkā |
| 72042 | IEC 62366-1:2015/Cor 1:2016 | Medical devices — Part 1: Application of usability engineering to medical devices — Technical Corrigendum 1 | Standarts spēkā |
| 72704 | ISO 14971:2019 | Medical devices — Application of risk management to medical devices | 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 |
| 69729 | ISO 18250-7:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 7: Connectors for intravascular infusion | 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 |
| 69731 | ISO 18250-6:2019 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 6: Neural applications | Standarts spēkā |
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 67943 | ISO 20417:2021 | Medical devices — Information to be supplied by the manufacturer | Standarts spēkā |
| 54146 | IEC/TR 80002-1:2009 | Medical device software — Part 1: Guidance on the application of ISO 14971 to medical device software | Standarts spēkā |
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