CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 62263 | EN ISO 17511:2021 | In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO/DIS 17511:2019) | Standarts spēkā |
| 5116 | LVS EN 12322:2001/A1:2002 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Standarts spēkā |
| 61692 | LVS EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | Standarts spēkā |
| 61686 | EN ISO 20186-3:2019 | Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019) | Standarts spēkā |
| 70517 | LVS EN ISO 20184-3:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO 20184-3:2021) | Standarts spēkā |
| 76941 | CEN ISO/TS 7552-1:2024 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 1: Isolated RNA (ISO/TS 7552-1:2024) | Standarts spēkā |
| 61692 | EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | Standarts spēkā |
| 67447 | LVS CEN/TS 17688-1:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA | Standarts spēkā |
| 5106 | LVS EN 13975:2003 | Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects | Standarts spēkā |
| 5107 | LVS EN 13641:2003 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Standarts spēkā |
Displaying 61-70 of 277 results.