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EN ISO 18113-1

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

Free. One email when its cessation date is set, moves, or the listing changes — instead of re-reading the whole annex every month.

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

JSON: /api/v1/standard/en-iso-18113-1.json

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