Registration number (WIID)Project No.TitleStatus
39727LVS EN ISO 23640:2013In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Atcelts
5102LVS EN 14820:2005Single-use containers for human venous blood specimen collectionAtcelts
27620LVS EN ISO 18113-5:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
37589LVS EN ISO 18113-1:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
37593LVS EN ISO 18113-5:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
23415LVS EN ISO 20776-1:2007Clinical 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 diseasesAtcelts
24452LVS EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competenceAtcelts
5105LVS EN ISO 17511:2003In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materialsAtcelts
62239LVS CEN/TS 17305:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNAAtcelts
62543LVS EN ISO 22870:2017Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
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