{"standard":"EN ISO 13408-5","listings":[{"edition":"EN ISO 13408-5:2011","list":"uk-in-vitro-diagnostic-medical-devices","list_name":"UK IVD (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-in-vitro-diagnostic-medical-devices"},{"edition":"EN ISO 13408-5:2011","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)","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"}