EN ISO 18113-2in-force
EN ISO 18113-2:2024 — In vitro diagnostic devices - labelling - Part 2: reagents for professional use
EN ISO 18113-2:2024
Applies from 2026-01-30
Summary
IVDR (EU) 2017/746 harmonised standard: In vitro diagnostic devices - labelling - Part 2: reagents for professional use.
Scope
EU harmonised standard under Medical Devices Regulation (EU) 2017/745 — In vitro diagnostic devices - labelling - Part 2: reagents for professional use.
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