EN ISO 18113-1in-force
EN ISO 18113-1:2011 — In vitro diagnostic medical devices - Labelling - Part 1: Terms, definitions and general requirements
EN ISO 18113-1:2011
Applies from 2011-01-01
Summary
EU harmonised standard EN ISO 18113-1:2011: In vitro diagnostic medical devices - Labelling - Part 1: Terms, definitions and general requirements.
Scope
IVDR (Regulation (EU) 2017/746) / MDD harmonised standard — In vitro diagnostic medical devices - Labelling - Part 1: Terms, definitions and general requirements.
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