CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5102 | LVS EN 14820:2005 | Single-use containers for human venous blood specimen collection | Atcelts |
| 27620 | LVS EN ISO 18113-5:2010 | 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 |
| 37589 | LVS EN ISO 18113-1:2012 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) | 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 |
| 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 |
| 24452 | LVS EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence | Atcelts |
| 5105 | LVS EN ISO 17511:2003 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials | Atcelts |
| 29669 | LVS EN ISO 15189:2013 A | Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) | Atcelts |
| 22397 | EN 13612:2002/AC:2002 | Performance evaluation of in vitro diagnostic medical devices | Izstrādē |
| 73607 | FprEN ISO 15193 | In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026) | Izstrādē |
Displaying 201-210 of 277 results.