{"standard":"EN 62366","listings":[{"edition":"EN 62366:2008","list":"uk-in-vitro-diagnostic-medical-devices","list_name":"UK IVD (designated)","jurisdiction":"UK","title":"Medical devices - Application of usability engineering to medical devices","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"","withdrawal":"17/01/2026","source":"https://www.gov.uk/government/publications/designated-standards-in-vitro-diagnostic-medical-devices"},{"edition":"EN 62366:2008","list":"uk-medical-devices","list_name":"UK Medical Devices (designated)","jurisdiction":"UK","title":"Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)","annex":"S.I. 2002/618","pc_start":"01/01/2021","restriction":"Informative Note: This standard does not necessarily cover the requirements introduced into the Medical Devices Regulations 2002 by S.I. 2008/2936 (which implemented Directive 2007/747/EC). Manufacturers are advised to check whether all relevant essential requirements are appropriately covered.","withdrawal":"","source":"https://www.gov.uk/government/publications/designated-standards-medical-devices"}],"events":[],"generated":"2026-08-16 23:54 UTC"}