{"standard":"EN ISO 14160","listings":[{"edition":"EN ISO 14160:2021","list":"mdr","list_name":"Medical Devices Regulation","jurisdiction":"EU","title":"Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2020)","annex":"ANNEX","source":"https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02021D1182-20260617"},{"edition":"EN ISO 14160:2021","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices","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":"2022-01-05","type":"added","ref":"EN ISO 14160:2021","leg_slug":"mdr","leg_name":"Medical Devices Regulation"}],"generated":"2026-08-16 23:54 UTC"}