# ISO 18113-1:2009 — Withdrawn and superseded ISO standards

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(labelling) — Part 1: Terms, definitions and general requirements; status code is 9599; successor is ISO 18113-1:2022; withdrawn / published date is 2009-12-09, recorded from its source on 2026-08-05.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: appears in the quote below)_
- **Item title:** In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements _(verified: appears in the quote below)_
- **Status code:** 9599 _(verified: appears in the quote below)_
- **Successor:** ISO 18113-1:2022
- **Withdrawn / published date:** 2009-12-09 _(verified: appears in the quote below)_

## 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>"

## Source

- https://isopublicstorageprod.blob.core.windows.net/opendata/_latest/iso_deliverables_metadata/csv/iso_deliverables_metadata.csv

Last verified: 2026-08-05. Review by: 2027-02-01.
Part of [Withdrawn and superseded ISO standards](https://referencesource.org/iso-standard-supersessions/).