ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 43034 | ISO/NP TS 19218 | Medical devices — Nomenclature and system for adverse medical device event reporting | Izstrādē |
| 73778 | ISO/PWI TR 22740 | Devices incorporating small-bore connectors— recommended colour allocation for each application | Izstrādē |
| 25798 | ISO/WD 14970 | Medical devices — General aspects to be considered when developing standards for medical devices (replaced by ISO/IEC Guide 63) | Izstrādē |
| 88848 | IEC/CD TS 62366-2 | Medical devices — Part 2: Guidance on the application of usability engineering to medical devices | Izstrādē |
| 86271 | ISO/PWI 20375 | Medical devices — Post-market surveillance for manufacturers – additional example | Izstrādē |
| 38194 | ISO/PWI 14971-B | Medical devices — Application of risk management to medical devices — Part B: In vitro diagnostic medical devices | Izstrādē |
| 26497 | ISO/WD 15224 | Medical devices — Compendium of terms and definitions | Izstrādē |
| 38430 | ISO/NP 17692 | Medical devices — General requirements for safety and essential performance — Usability | Izstrādē |
| 40128 | ISO/CD 15223 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied | Izstrādē |
| 45964 | ISO/WD 10369-1 | Medical devices - Small bore connectors for liquids and gases in healthcare applications — Part 1: General requirements | Izstrādē |
Displaying 101-110 of 115 results.