CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 41040 | LVS CEN/TS 16835-3:2016 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma | Atcelts |
| 29759 | LVS EN ISO 23640:2012 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 24023 | LVS EN ISO 15197:2003 /AC:2005 | In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitus | Atcelts |
| 27619 | LVS EN ISO 18113-4:2010 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) | Atcelts |
| 5080 | LVS EN 12376:2000 | In vitro diagnostic medicaldevices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
| 5074 | LVS EN 12287:2000 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials | Atcelts |
| 5075 | LVS EN 829:2000 | In vitro diagnostic systems - Transport packages for medical and biological speciments - Requirements, tests | Atcelts |
| 5096 | LVS EN 1658:2000 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 5094 | LVS EN 591:1993 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 5098 | LVS EN 375:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
Displaying 131-140 of 275 results.