In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Standard [CURRENT]

UNE-EN ISO 18113-1:2025-01-22

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Publication date
2025-01-22
Original language
Spanish
Pages
71

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Publication date
2025-01-22
Original language
Spanish
Pages
71
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