Registration number (WIID)Project No.TitleStatus
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
5080LVS EN 12376:2000In vitro diagnostic medicaldevices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
37591LVS EN ISO 18113-3:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)Atcelts
27620EN ISO 18113-5:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2009)Atcelts
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
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
29669LVS EN ISO 15189:2013 AMedical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)Atcelts
37590EN ISO 18113-2:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)Atcelts
24023LVS EN ISO 15197:2003 /AC:2005In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
41043CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
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