{"standard":"EN ISO 10993-10","listings":[{"edition":"EN ISO 10993-10:2023","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Biological evaluation of medical devices – Part 10: Tests for skin sensitisation (ISO 10993-10:2021)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"},{"edition":"EN ISO 10993-10:2023","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Biological evaluation of medical devices – Part 10: Tests for skin sensitisation","annex":"S.I. 2002/618","pc_start":"17/01/2026","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"}],"events":[{"date":"2023-07-05","type":"added","ref":"EN ISO 10993-10:2023","leg_slug":"mdr","leg_name":"Medical Devices Regulation"}],"generated":"2026-08-17 02:41 UTC"}