{"standard":"EN ISO 13408-2","listings":[{"edition":"EN ISO 13408-2:2011","list":"uk-in-vitro-diagnostic-medical-devices","list_name":"UK IVD (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"30/09/2021","source":"https://www.gov.uk/government/publications/designated-standards-in-vitro-diagnostic-medical-devices"},{"edition":"EN ISO 13408-2:2011","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)","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 13408-2:2018","list":"uk-in-vitro-diagnostic-medical-devices","list_name":"UK IVD (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)","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 13408-2:2018","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)","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":"2026-08-17 02:41 UTC"}