CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 64861 | CEN/TR 17223:2018 | Guidance on the relationship between EN ISO 13485: 2016 (Medical devices - Quality management systems - Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation | Atcelts |
| 24145 | CEN/TR 15133:2005 | Nomenclature - Collective terms and codes for groups of medical devices | Atcelts |
| 24416 | CEN ISO/TR 14969:2005 | Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004) | Atcelts |
| 38595 | EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 18856 | EN ISO 14971:2000 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 24766 | EN 980:2008 | Symbols for use in the labelling of medical devices | Atcelts |
| 12987 | CR 13217:1998 | Nomenclature system for medical devices for the purpose of regulatory data exchange - Rationale | Atcelts |
| 21726 | EN ISO 15225:2000/A1:2004 | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange - Amendment 1 (ISO 15225:2000/A1:2004) | Atcelts |
| 21072 | EN ISO 14971:2000/AC:2002 | Medical devices - Application of risk management to medical devices (ISO 14971:2000) | Atcelts |
| 21479 | EN ISO 14971:2000/A1:2003 | Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AM1:2003) | Atcelts |
Displaying 71-80 of 141 results.