CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 73608 | prEN ISO 15194 | In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023) | Izstrādē |
| 29669 | EN ISO 15189:2012 | Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011) | Atcelts |
| 5096 | EN 1658:1996 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 33817 | EN ISO 15197:2013 | In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013) | Atcelts |
| 67447 | CEN/TS 17688-1:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA | Atcelts |
| 5112 | EN 14254:2004 | In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans | Atcelts |
| 67448 | CEN/TS 17688-3:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNA | Atcelts |
| 5075 | EN 829:1996 | In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, tests | Atcelts |
| 5094 | EN 591:1994 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 37593 | EN ISO 18113-5:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009) | Atcelts |
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