CEN/TC 140
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
39727 | LVS EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
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 |
62239 | LVS CEN/TS 17305:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA | Atcelts |
62543 | LVS EN ISO 22870:2017 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016) | Atcelts |
Displaying 141-150 of 272 results.