{"standard":"EN IEC 60601-2-83","listings":[{"edition":"EN IEC 60601-2-83:2020","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"}],"events":[{"date":"2022-01-05","type":"added","ref":"EN IEC 60601-2-83:2020","leg_slug":"mdr","leg_name":"Medical Devices Regulation"}],"generated":"2026-08-17 02:41 UTC"}