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Homepage>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)
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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)

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
DESCRIPTION

This standard 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) is classified in these ICS categories:

  • 11.100.10
Categories: