11.100.10 In vitro diagnostic test systems
Displaying 49-60 of 120 results.
LVS CEN/TS 17688-3:2022
technical specification (TS)
EN
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNA
21.25 €
LVS CEN/TS 17742:2022
technical specification (TS)
EN
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
18.53 €
LVS CEN/TS 17747:2022
technical specification (TS)
EN
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
19.44 €
LVS CEN/TS 17811:2022
technical specification (TS)
EN
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
17.61 €
LVS CEN/TS 17981-1:2023
technical specification (TS)
EN
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examination
26.12 €
LVS CEN/TS 17981-2:2023
technical specification (TS)
EN
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination
26.12 €
ISO/TR 18112:2006
technical report (TR)
EN
Clinical laboratory testing and in vitro diagnostic test systems In vitro diagnostic medical devices for professional use Summary of regulatory requirements for information supplied by the manufacturer
68.85 €
ISO 18113-1:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
68.85 €
ISO 18113-1:2022
standard
EN
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
210.78 €
ISO 18113-2:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
68.85 €
ISO 18113-2:2022
standard
EN
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
68.85 €
ISO 18113-3:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
68.85 €