Registration number (WIID)Project No.TitleStatus
5098EN 375:2001Information supplied by the manufacturer with in vitro diagnostic reagents for professional useAtcelts
24023EN ISO 15197:2003/AC:2005In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
62239CEN/TS 17305:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNAAtcelts
65452CEN/TS 17390-2:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNAAtcelts
5096LVS EN 1658:2000Requirements for marking of in vitro diagnostic instrumentsAtcelts
5094LVS EN 591:1993In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
5098LVS EN 375:2001In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testingAtcelts
25659EN ISO 15189:2007Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5095LVS EN 592:2001In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for home useAtcelts
5069LVS EN 928:2001In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devicesAtcelts
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