Registration number (WIID)Project No.TitleStatus
5102EN 14820:2004Single-use containers for human venous blood specimen collectionAtcelts
27616EN ISO 18113-1:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/FDIS 18113-1:2009)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
37591EN ISO 18113-3:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)Atcelts
65450LVS CEN/TS 17390-1:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNAAtcelts
65452LVS CEN/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
65451LVS CEN/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
81455prEN ISO 25379-2In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 2: Human RNA examinationIzstrādē
81156prEN ISO 15197 revIn vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
68789EN ISO 20166-4:2021Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO/DIS 20166-4:2020)Izstrādē
Displaying 201-210 of 277 results.