CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 33817 | LVS 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 |
| 5098 | LVS EN 375:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
| 37208 | LVS EN ISO 16256:2013 | Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012) | Atcelts |
| 24452 | LVS EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence | Atcelts |
| 23415 | LVS EN ISO 20776-1:2007 | Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Atcelts |
| 5094 | LVS EN 591:1993 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 5096 | LVS EN 1658:2000 | Requirements for marking of in vitro diagnostic instruments | Atcelts |
| 37593 | LVS EN ISO 18113-5:2012 | 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 |
| 5069 | EN 928:1995 | In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices | Atcelts |
| 5067 | LVS EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
Displaying 81-90 of 272 results.