Registration number (WIID)Project No.TitleStatus
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
31718ISO 18153:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materialsAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
40987ISO 18113-4:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testingAtcelts
40986ISO 18113-3:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
40984ISO 18113-1:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsAtcelts
67022ISO 17822:2020In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guideStandarts spēkā
79378ISO 17593:2022Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyStandarts spēkā
36872ISO 17593:2007Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyAtcelts
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