ISO 18113-3:2009
For ISO 18113-3:2009, item title is In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use; status code is 9599; successor is ISO 18113-3:2022; withdrawn / published date is 2009-12-09, recorded from its source on 2026-08-05.
- Identifier
- ISO 18113-3:2009 verified
- Item title
- In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use verified
- Status code
- 9599 verified
- Successor
- ISO 18113-3:2022
- Withdrawn / published date
- 2009-12-09 verified
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What the source says
40986,IS,,ISO 18113-3:2009,In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use,Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 3: Instruments de diagnostic in vitro à usage professionnel,2009-12-09,1,['11.100.10'],ISO/TC 212,9599,,[79868],"['en','fr','ru']",9,"<p>ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of <i>in vitro</i> dignostic (IVD)<i> </i>instruments for professional use.</p><p>ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD<i> </i>instruments for
— 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