Registration number (WIID)Project No.TitleStatus
70932EN ISO 18113-4:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)Standarts spēkā
61693LVS EN ISO 20166-1:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018)Standarts spēkā
70933EN ISO 18113-5:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)Standarts spēkā
70931EN ISO 18113-3:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)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
70929LVS EN ISO 18113-1:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)Standarts spēkā
70930EN ISO 18113-2:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)Standarts spēkā
61390EN ISO 15195:2019Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO/DIS 15195:2018)Standarts spēkā
5103LVS EN 13612:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
5090LVS EN 1659:1996In vitro diagnostic systems - Culture media for microbiology - Terms and definitionsStandarts spēkā
Displaying 11-20 of 275 results.