Registration number (WIID)Project No.TitleStatus
5116LVS EN 12322:2001/A1:2002In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture mediaStandarts spēkā
70933LVS EN 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
75465LVS CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
64279LVS EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Standarts spēkā
70931LVS EN 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
70930LVS EN 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
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
61695LVS EN ISO 20184-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 2: Isolated proteins (ISO 20184-2:2018)Standarts spēkā
61686LVS EN ISO 20186-3:2020Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)Standarts spēkā
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