ISO/TC 210
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 60044 | ISO/TR 80002-2:2017 | Medical device software — Part 2: Validation of software for medical device quality systems | Standarts spēkā |
| 67942 | ISO/TR 20416:2020 | Medical devices — Post-market surveillance for manufacturers | Standarts spēkā |
| 50733 | IEC 80369-5:2016 | Small-bore connectors for liquids and gases in healthcare applications — Part 5: Connectors for limb cuff inflation applications | Standarts spēkā |
| 31550 | ISO 14971:2000 | Medical devices — Application of risk management to medical devices | 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 |
| 36029 | ISO 14971:2000/Amd 1:2003 | Medical devices — Application of risk management to medical devices — Amendment 1: Rationale for requirements | Atcelts |
| 50729 | ISO/IEC Guide 63:2012 | Guide to the development and inclusion of safety aspects in International Standards for medical devices | Atcelts |
| 30163 | ISO/TR 16142:1999 | Medical devices — Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices | Atcelts |
| 38062 | ISO 15223:2000/Amd 2:2004 | Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Amendment 2 | Atcelts |
| 22098 | ISO 13485:1996 | Quality systems Medical devices Particular requirements for the application of ISO 9001 | Atcelts |
Displaying 31-40 of 114 results.