Registration number (WIID)Project No.TitleStatus
27619EN ISO 18113-4:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/FDIS 18113-4:2009)Atcelts
5067EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
5108EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
41040CEN/TS 16835-3:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasmaAtcelts
41033CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
27618LVS EN ISO 18113-3:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)Atcelts
64590CEN/TS 16826-3:2018Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNAAtcelts
5080EN 12376:1999In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
27617LVS EN ISO 18113-2:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)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
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