Registration number (WIID)Project No.TitleStatus
23415LVS EN ISO 20776-1:2007Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesAtcelts
5075LVS EN 829:2000In vitro diagnostic systems - Transport packages for medical and biological speciments - Requirements, testsAtcelts
5067LVS EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
41033CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
37593LVS EN ISO 18113-5:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
37589LVS EN ISO 18113-1:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
5074LVS EN 12287:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsAtcelts
27620LVS EN ISO 18113-5:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
5102LVS EN 14820:2005Single-use containers for human venous blood specimen collectionAtcelts
5080LVS EN 12376:2000In vitro diagnostic medicaldevices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
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