Registration number (WIID)Project No.TitleStatus
5101EN 592:2002Instructions for use for in vitro diagnostic instruments for self-testingAtcelts
5098EN 375:2001Information supplied by the manufacturer with in vitro diagnostic reagents for professional useAtcelts
37593EN ISO 18113-5:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
64590CEN/TS 16826-3:2018Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNAAtcelts
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
41045LVS CEN/TS 16835-2:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
41033CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
29669LVS EN ISO 15189:2013 AMedical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)Atcelts
65451CEN/TS 17390-3:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC stainingAtcelts
62543LVS EN ISO 22870:2017Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
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