{"standard":"EN ISO 17664","listings":[{"edition":"EN ISO 17664:2004","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"},{"edition":"EN ISO 17664:2017","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"}],"events":[],"generated":"2026-08-16 23:54 UTC"}