CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32013 | prEN ISO 13485 rev | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) | Izstrādē |
| 66179 | prEN ISO 80369-3 rev | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications (ISO 80369-3:2016) | Izstrādē |
| 71616 | EN ISO 80369-3:2016/A1:2022 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/Amd 1:2019) | Izstrādē |
| 69482 | EN ISO 15223-1:2016/FprA11 | Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016) | Izstrādē |
| 40444 | LVS EN 1041+A1:2014 | Information supplied by the manufacturer of medical devices | Atcelts |
| 12983 | LVS CR 14230:2003 | Global medical device nomenclature for the purpose of regulatory data exchange | Atcelts |
| 38595 | LVS EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | 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 |
| 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 |
| 28921 | LVS EN ISO 13485:2003 /AC:2007 | Medical devices - Quality management systems - Requirements for regulatory purposes | Atcelts |
Displaying 21-30 of 144 results.