Registration number (WIID)Project No.TitleStatus
70517LVS EN ISO 20184-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO 20184-3:2021)Standarts spēkā
27354LVS EN ISO 15194:2009In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)Standarts spēkā
67448LVS CEN/TS 17688-3:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNAStandarts spēkā
5116LVS EN 12322:2001/A1:2002In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture mediaStandarts spēkā
61692LVS EN ISO 6710:2017Single-use containers for human venous blood specimen collection (ISO 6710:2017)Standarts spēkā
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
61687LVS EN ISO 20186-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)Standarts spēkā
79624prEN ISO 23640In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO/DIS 23640:2026)Aptauja
26409EN ISO 20776-2:2007Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices (ISO 20776-2:2007)Atcelts
41044LVS CEN/TS 16827-3:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 3: Isolated DNAAtcelts
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