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>UNE EN ISO 18113-4:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)
sklademVydáno: 2025-01-22
UNE EN ISO 18113-4:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)

UNE EN ISO 18113-4:2025

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 4: Reactivos para diagnóstico in vitro para autodiagnóstico. (ISO 18113-4:2022).

Formát
Dostupnost
Cena a měna
Španělsky PDF
K okamžitému stažení
2083 Kč
Španělsky Tisk
Skladem
2083 Kč
Anglicky PDF
K okamžitému stažení
2499 Kč
Anglicky Tisk
Skladem
2499 Kč
Označení normy:UNE EN ISO 18113-4:2025
Počet stran:25
Vydáno:2025-01-22
Status:Norma
Počet stran (Španělsky):25
Počet stran (Anglicky):25
Popis

This standard UNE EN ISO 18113-4:2025 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022) is classified in these ICS categories:

  • 11.100.10
: