CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5112 | LVS EN 14254:2004 | In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans | Atcelts |
| 41043 | CEN/TS 16945:2016 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma | Atcelts |
| 62543 | LVS EN ISO 22870:2017 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016) | Atcelts |
| 5096 | LVS EN 1658:2000 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 27617 | EN ISO 18113-2:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/FDIS 18113-2:2009) | Atcelts |
| 27620 | EN ISO 18113-5:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2009) | Atcelts |
| 29669 | LVS EN ISO 15189:2013 A | Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) | Atcelts |
| 5094 | LVS EN 591:1993 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 65450 | CEN/TS 17390-1:2020 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA | Atcelts |
| 5100 | EN 591:2001 | Instructions for use for in vitro diagnostic instruments for professional use | Atcelts |
Displaying 91-100 of 276 results.