CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 59550 | LVS EN ISO 15223-1:2017 | Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2016-12-15) | Atcelts |
| 22133 | EN ISO 13485:2003 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Atcelts |
| 39825 | LVS EN ISO 15225:2016 | Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016) | Atcelts |
| 40444 | EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices | Atcelts |
| 12985 | LVS EN ISO 15225:2001 | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange | Atcelts |
| 24162 | EN ISO 14971:2007 | Medical devices - Application of risk management to medical devices (ISO 14971:2007) | Atcelts |
| 64861 | LVS 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 |
| 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 |
Displaying 71-80 of 140 results.