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EN ISO 18113-1

2 current listing(s) — 1 EU harmonised, 1 UK designated.

Current listings

EditionListTitlePresumption from Withdrawal / cessation
EN ISO 18113-1:2011UK UK IVD (designated)In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirem01/01/2021source
EN ISO 18113-1:2024EU IVD RegulationIn vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requiresource

Timeline

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