Registration number (WIID)Project No.TitleStatus
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
25659LVS EN ISO 15189:2007 AMedical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
33817LVS EN ISO 15197:2013In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)Atcelts
41040LVS CEN/TS 16835-3:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasmaAtcelts
5073LVS EN 12286:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
41041LVS CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
5102EN 14820:2004Single-use containers for human venous blood specimen collectionAtcelts
5099LVS EN 376:2003Information supplied by the manufacturer with in vitro diagnostic reagents for self-testingAtcelts
5107LVS EN 13461:2003Packaging - Cylindrical flexible laminated tubes - Dimensions and tolerancesAtcelts
5112LVS EN 14254:2004In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humansAtcelts
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