ISO 18113-1:2009
For ISO 18113-1:2009, item title is In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements; status code is 9599; successor is ISO 18113-1:2022; withdrawn / published date is 2009-12-09, recorded from its source on 2026-08-05.
- Identifier
- ISO 18113-1:2009 verified
- Item title
- In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements verified
- Status code
- 9599 verified
- Successor
- ISO 18113-1:2022
- Withdrawn / published date
- 2009-12-09 verified
Verified
Review by
What the source says
40984,IS,,ISO 18113-1:2009,"In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements","Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 1: Termes, définitions et exigences générales",2009-12-09,1,['11.100.10'],ISO/TC 212,9599,,[79866],"['en','fr','ru']",49,"<p>ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of <i>in vitro</i> diagnostic (IVD) medical devices.</p>"
— isopublicstorageprod.blob.core.windows.net, retrieved 2026-08-05
Source
- isopublicstorageprod.blob.core.windows.nethttps://isopublicstorageprod.blob.core.windows.net/opendata/_latest/iso_deliverables_metadata/csv/iso_deliverables_metadata.csv