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 |
| 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 |
| 64555 | EN 80369-5:2016/AC:2017-02 | Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications | Standarts spēkā |
| 64555 | LVS EN 80369-5:2016/AC:2017-02 | Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications | |
| 64227 | EN ISO 80369-3:2016/prA2 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 2 (ISO 80369-3:2016/DAmd 2:2017) | Izstrādē |
| 64226 | EN ISO 80369-3:2016/prA1 | Small-bore connectors for liquids and gases in healthcare applications - Part 3: Connectors for enteral applications - Amendment 1 (ISO 80369-3:2016/DAmd 1:2017) | Izstrādē |
| 64029 | LVS EN ISO 13485:2016/AC:2017 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
| 64029 | EN ISO 13485:2016/AC:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Atcelts |
| 63920 | LVS EN ISO 14971:2020 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
| 63920 | EN ISO 14971:2019 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
Displaying 41-50 of 139 results.