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>UNE EN ISO 18113-3:2025 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)
sklademVydáno: 2025-01-22
UNE EN ISO 18113-3:2025 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)

UNE EN ISO 18113-3:2025

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 3: Instrumentos para diagnóstico in vitro para uso profesional. (ISO 18113-3:2022).

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Označení normy:UNE EN ISO 18113-3:2025
Počet stran:23
Vydáno:2025-01-22
Status:Norma
Počet stran (Španělsky):25
Popis

UNE EN ISO 18113-3:2025

This document specifies requirements for information supplied by the manufacturer of IVD instruments intended for professional use. This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This document can also be applied to accessories. This document does not apply to: a) instructions for instrument servicing or repair; b) IVD reagents, including calibrators and control materials for use in control of the reagent; c) IVD instruments for self-testing.

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