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Homepage>UNE EN ISO 18113-2:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

UNE EN ISO 18113-2:2025

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 2: Reactivos para diagnóstico in vitro para uso profesional. (ISO 18113-2:2022).

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Označení normy:	UNE EN ISO 18113-2:2025
Počet stran:	25
Vydáno:	2025-01-22
Status:	Norma

DESCRIPTION

This standard UNE EN ISO 18113-2:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022) is classified in these ICS categories:

11.100.10

Categories:

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