CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5098 | EN 375:2001 | Information supplied by the manufacturer with in vitro diagnostic reagents for professional use | Atcelts |
| 5067 | EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
| 5090 | EN 1659:1996 | In vitro diagnostic systems - Culture media for microbiology - Terms and definitions | Izstrādē |
| 5096 | EN 1658:1996 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 29047 | EN 14820:2004/prA1 | Single-use containers for human venous blood specimen collection | Izstrādē |
| 5102 | EN 14820:2004 | Single-use containers for human venous blood specimen collection | Atcelts |
| 5112 | EN 14254:2004 | In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans | Atcelts |
| 5111 | EN 14136:2004 | Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures | Izstrādē |
| 5106 | EN 13975:2003 | Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects | Izstrādē |
| 5107 | EN 13641:2002 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Izstrādē |
Displaying 221-230 of 274 results.