CEN/CLC/TC 3
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
24766 | LVS EN 980:2008 | Symbols for use in the labelling of medical devices | Atcelts |
12983 | CR 14230:2001 | Global medical device nomenclature for the purpose of regulatory data exchange (identical to ISO/TS 20225:2001) | Atcelts |
38536 | EN ISO 13485:2012/AC:2012 | Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009) | Atcelts |
64029 | LVS EN ISO 13485:2016/AC:2017 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
39370 | LVS EN ISO 80369-7:2017 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016) | Atcelts |
64029 | EN ISO 13485:2016/AC:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
79260 | prEN ISO 20417 | Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024) | Aptauja slēgta |
68559 | LVS EN ISO 15223-1:2021 | Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021) | Standarts spēkā |
69481 | LVS EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
66261 | LVS CEN ISO/TR 20416:2020 | Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020) | Standarts spēkā |
Displaying 91-100 of 140 results.