ISO/TC 212

Reģistrācijas numurs (WIID)Projekta Nr.NosaukumsStatuss
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts spēkā
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 18113-5:2009Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 5: Instruments de diagnostic in vitro pour auto-testsAtcelts
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 18113-2:2009Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 2: Réactifs de diagnostic in vitro à usage professionnelAtcelts
40984ISO 18113-1:2009Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 1: Termes, définitions et exigences généralesAtcelts
67022ISO 17822:2020In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guideAtcelts
79378ISO 17593:2022Laboratoires d'analyses de biologie médicale et dispositifs médicaux de diagnostic in vitro — Exigences relatives aux systèmes d'autosurveillance des traitements par anti-coagulant orauxStandarts spēkā
Attēlo no 111. līdz 120. no pavisam 143 ieraksta(-iem).