CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5100 | EN 591:2001 | Instructions for use for in vitro diagnostic instruments for professional use | Atcelts |
| 5099 | EN 376:2002 | Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing | Atcelts |
| 64590 | LVS CEN/TS 16826-3:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNA | Atcelts |
| 5096 | EN 1658:1996 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 5068 | EN 376:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for self-testing | Atcelts |
| 5075 | EN 829:1996 | In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, tests | Atcelts |
| 62543 | EN ISO 22870:2016 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO/FDIS 22870:2016) | Atcelts |
| 41043 | LVS CEN/TS 16945:2016 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma | Atcelts |
| 41047 | LVS CEN/TS 16826-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteins | Atcelts |
| 37591 | EN ISO 18113-3:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009) | Atcelts |
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