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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)
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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Španělsky PDF
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143.54 €
Španělsky Hardcopy
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Anglicky PDF
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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 |
DESCRIPTION
This standard 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) is classified in these ICS categories:
- 11.100.10
- 01.040.11
Categories: