CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32012 | LVS EN ISO 14971:2009 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) | Atcelts |
| 30210 | LVS EN ISO 15225:2010 | Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2010) | Atcelts |
| 31251 | LVS EN ISO 80369-1:2011 | Small bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2010) | Atcelts |
| 12988 | LVS EN 980:2003 | Graphical symbols for use in the labelling of medical devices | Atcelts |
| 26098 | LVS EN 15546-1:2008 | Small bore connectors for liquids and gases in healthcare applications - Part 1 - General Requirements | Atcelts |
| 12987 | LVS CR 13217:2001 | Nomenclature system for medical devices for the purpose of regulatory data exchange - Rationale | 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 |
| 39825 | LVS EN ISO 15225:2016 | Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016) | Atcelts |
| 12985 | LVS EN ISO 15225:2001 | Nomenclature - Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange | 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 |
Displaying 101-110 of 140 results.