Registration number (WIID)Project No.TitleStatus
70518LVS EN ISO 6717:2021In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)Standarts spēkā
68138LVS CEN/TS 17742:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasmaStandarts spēkā
76942CEN ISO/TS 7552-3:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining (ISO/TS 7552-3:2024)Standarts spēkā
5103LVS EN 13612:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
5080LVS EN 12376:2000In vitro diagnostic medicaldevices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
5074LVS EN 12287:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsAtcelts
27619LVS EN ISO 18113-4:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
5075LVS EN 829:2000In vitro diagnostic systems - Transport packages for medical and biological speciments - Requirements, testsAtcelts
5108EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
24023LVS EN ISO 15197:2003 /AC:2005In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
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