11.100.10 In vitro diagnostic test systems
Displaying 49-60 of 116 results.
LVS CEN/TS 17981-1:2023
technical specification (TS)
EN
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examination
22.71 €
LVS CEN/TS 17981-2:2023
technical specification (TS)
EN
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination
22.71 €
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
48.19 €
ISO 18113-1:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
48.19 €
ISO 18113-1:2022
standard
EN
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
147.55 €
ISO 18113-2:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
48.19 €
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
48.19 €
ISO 18113-3:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
48.19 €
ISO 18113-3:2022
standard
EN
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
48.19 €
ISO 18113-4:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
48.19 €
ISO 18113-4:2022
standard
EN
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
48.19 €
ISO 18113-5:2009
standard
EN
In vitro diagnostic medical devices Information supplied by the manufacturer (labelling)
48.19 €