Registration number (WIID)Project No.TitleStatus
24452LVS EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competenceAtcelts
41045CEN/TS 16835-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
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
5095LVS EN 592:2001In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for home useAtcelts
29759LVS EN ISO 23640:2012In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Atcelts
27618EN ISO 18113-3:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2009)Atcelts
37589EN ISO 18113-1:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
37590EN ISO 18113-2:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)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
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
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