Registration number (WIID)Project No.TitleStatus
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
64590LVS CEN/TS 16826-3:2018Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNAAtcelts
41043LVS CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
5067EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
5080EN 12376:1999In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
25659LVS EN ISO 15189:2007 AMedical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5096EN 1658:1996Requirements for marking of in vitro diagnostic instrumentsAtcelts
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
5108LVS EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
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