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>UNE EN ISO 18113-1:2025 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)
sklademVydáno: 2025-01-22
UNE EN ISO 18113-1:2025 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

UNE EN ISO 18113-1:2025

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 1: Términos, definiciones y requisitos generales. (ISO 18113-1:2022).

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Označení normy:UNE EN ISO 18113-1:2025
Počet stran:66
Vydáno:2025-01-22
Status:Norma
Počet stran (Španělsky):71
Popis

UNE EN ISO 18113-1:2025

This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This document does not address language requirements since that is the domain of national laws and regulations. This document does not apply to: a) IVD medical devices for performance evaluation (e.g. for investigational use only); b) packaging list; c) material safety data sheets / Safety Data Sheets; d) marketing information (consistent with applicable legal requirements).

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