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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro…

Overview EN ISO 18113-2:2024 - "In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use" is the CEN-adop…

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro…

Overview EN ISO 18113-2:2024 - "In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use" is the CEN-adop…

Tracked Changes. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). I…

In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) - In vitro diagnost…

1 Scope This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use. This part of ISO 18113 also applies to information supplied by…

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro…

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

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro…

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnosti…