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

Fecha Anulación:

2009-12-09 / Withdrawn

ICS:

11.100.10 - In vitro diagnostic test systems.

Committee:

ISO/TC 212 - Clinical laboratory testing and in vitro diagnostic test systems

Relación con otras normas ISO:

Es anulada por: ISO 18113-1:2022

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This standard is available in:

Digital format

Ingles / Frances