In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

Standard [CURRENT]

UNE-EN ISO 18113-2:2025-01-22

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)

Publication date
2025-01-22
Original language
Spanish
Pages
28

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Publication date
2025-01-22
Original language
Spanish
Pages
28
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