ISO/TC 210
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
55589 | ISO/TS 19218-1:2011 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes | Atcelts |
55590 | ISO/TS 19218-2:2012 | Medical devices — Hierarchical coding structure for adverse events — Part 2: Evaluation codes | Atcelts |
58011 | ISO 80369-7:2016 | Small-bore connectors for liquids and gases in healthcare applications — Part 7: Connectors for intravascular or hypodermic applications | Atcelts |
58085 | ISO/TS 19218-1:2011/Amd 1:2013 | Medical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codes — Amendment 1 | Atcelts |
59587 | ISO/TR 24971:2013 | Medical devices — Guidance on the application of ISO 14971 | Atcelts |
59752 | ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes | Standarts spēkā |
60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
61174 | ISO/NP 16142 | Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices | Izstrādē |
61895 | ISO 18250-3:2018 | Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 3: Enteral applications | Standarts spēkā |
62780 | IEC 62366:2007/Amd 1:2014 | Medical devices — Application of usability engineering to medical devices — Amendment 1 | Atcelts |
Displaying 51-60 of 114 results.