{"standard":"EN ISO 17665","listings":[{"edition":"EN ISO 17665:2024","list":"ivdr","list_name":"IVD Regulation","jurisdiction":"EU","title":"Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1195-20260617"},{"edition":"EN ISO 17665:2024","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Sterilization of health care products – Moist heat – Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"}],"events":[{"date":"2026-01-30","type":"added","ref":"EN ISO 17665:2024","leg_slug":"mdr","leg_name":"Medical Devices Regulation"},{"date":"2026-01-30","type":"added","ref":"EN ISO 17665:2024","leg_slug":"ivdr","leg_name":"IVD Regulation"}],"generated":"2026-08-16 23:54 UTC"}