{"standard":"EN ISO 10993-23","listings":[{"edition":"EN ISO 10993-23:2021","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"},{"edition":"EN ISO 10993-23:2021","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Biological evaluation of medical devices - Part 23: Tests for irritation","annex":"S.I. 2002/618","pc_start":"17/01/2026","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"}],"events":[],"generated":"2026-08-17 02:41 UTC"}