Reference Source

ISO 18113-4:2009

For ISO 18113-4:2009, item title is In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing; status code is 9599; successor is ISO 18113-4:2022; withdrawn / published date is 2009-12-17, recorded from its source on 2026-08-05.

Identifier
ISO 18113-4:2009 verified
Item title
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing verified
Status code
9599 verified
Successor
ISO 18113-4:2022
Withdrawn / published date
2009-12-17 verified
Sourceisopublicstorageprod.blob.core.windows.net
Verified
Review by
DatasetWithdrawn and superseded ISO standards

What the source says

40987,IS,,ISO 18113-4:2009,In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing,Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 4: Réactifs de diagnostic in vitro pour auto-tests,2009-12-17,1,['11.100.10'],ISO/TC 212,9599,,[79869],"['en','fr','ru']",10,"<p>ISO 18113-4:2009 specifies requirements for information supplied by the manufacturer of <i>in vitro</i> diagnostic (IVD) reagents for self-testing.</p><p>ISO 18113-4:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with I

isopublicstorageprod.blob.core.windows.net, retrieved 2026-08-05

Source

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