Registration number (WIID)Project No.TitleStatus
27617EN ISO 18113-2:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/FDIS 18113-2:2009)Atcelts
25659LVS EN ISO 15189:2007 AMedical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5098LVS EN 375:2001In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testingAtcelts
41043CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
37592EN ISO 18113-4:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
5108LVS EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
25659EN ISO 15189:2007Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5105EN ISO 17511:2003In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003)Atcelts
5113EN ISO 15195:2003Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003)Atcelts
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
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