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Homepage>UNE EN ISO 18113-5:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)
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sklademVydáno: 2025-01-22
UNE EN ISO 18113-5:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)

UNE EN ISO 18113-5:2025

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 5: Instrumentos para diagnóstico in vitro para autodiagnóstico. (ISO 18113-5:2022).

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Označení normy:UNE EN ISO 18113-5:2025
Počet stran:22
Vydáno:2025-01-22
Status:Norma
DESCRIPTION

This standard UNE EN ISO 18113-5:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022) is classified in these ICS categories:

  • 11.100.10
Categories:
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