CEN/CLC/TC 3
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 66700 | EN ISO 13485:2016/AC:2018 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 70256 | LVS EN ISO 80369-7:2021 | Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2021) | Standarts spēkā |
| 69481 | EN ISO 13485:2016/A11:2021 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
| 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 |
| 73006 | EN ISO 80369-2:2024 | Small-bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for respiratory applications (ISO 80369-2:2024, Corrected version 2025-06) | Standarts spēkā |
| 39366 | EN ISO 80369-6:2016 | Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neuraxial applications (ISO/IEC/DIS 80369-6:2014) | Standarts spēkā |
| 63920 | EN ISO 14971:2019 | Medical devices - Application of risk management to medical devices (ISO 14971:2019) | Standarts spēkā |
| 67368 | EN ISO 20417:2021 | Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12) | Standarts spēkā |
| 39363 | EN 80369-5:2016 | Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications | Standarts spēkā |
| 37957 | EN ISO 13485:2016 | Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) | Standarts spēkā |
Displaying 11-20 of 141 results.