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
5099EN 376:2002Information supplied by the manufacturer with in vitro diagnostic reagents for self-testingAtcelts
5104LVS EN 13640:2003Stability testing of in vitro diagnostic reagentsAtcelts
5107LVS EN 13461:2003Packaging - Cylindrical flexible laminated tubes - Dimensions and tolerancesAtcelts
5101LVS EN 592:2003Instructions for use for in vitro diagnostic instruments for self-testingAtcelts
5099LVS EN 376:2003Information supplied by the manufacturer with in vitro diagnostic reagents for self-testingAtcelts
37590LVS EN ISO 18113-2:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)Atcelts
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
41041LVS CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
67464CEN/TS 17811:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNAAtcelts
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