Registration number (WIID)Project No.TitleStatus
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
27619LVS EN ISO 18113-4:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
5112LVS EN 14254:2004In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humansAtcelts
24023LVS EN ISO 15197:2003 /AC:2005In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
27616LVS EN ISO 18113-1:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
29759LVS EN ISO 23640:2012In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)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
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
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
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
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