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ISO/TS 19218-2:2012WithdrawnMedical devices — Hierarchical coding structure for adverse events — Part 2: Evaluation codesTechnical Specification · Published 20 Mar 2012 · ISO/TC 210ISO/TS 19218-1:2011WithdrawnMedical devices — Hierarchical coding structure for adverse events — Part 1: Event-type codesTechnical Specification · Published 5 May 2011 · ISO/TC 210ISO/TS 19218:2005WithdrawnMedical devices — Coding structure for adverse event type and causeTechnical Specification · Published 3 Nov 2005 · ISO/TC 210ISO/TS 20225:2001WithdrawnGlobal medical device nomenclature for the purpose of regulatory data exchangeTechnical Specification · Published 22 Nov 2001 · ISO/TC 210ISO 20417:2021WithdrawnMedical devices — Information to be supplied by the manufacturerInternational Standard · Published 13 Apr 2021 · ISO/TC 210ISO/TR 24971:2013WithdrawnMedical devices — Guidance on the application of ISO 14971Technical Report · Published 19 Jun 2013 · ISO/TC 210IEC 62366:2007WithdrawnMedical devices — Application of usability engineering to medical devicesInternational Standard · Published 13 Nov 2007 · ISO/TC 210IEC/TR 80001-2-9:2017WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-9: Application guidance — Guidance for use of security assurance cases to demonstrate confidence in IEC/TR 80001-2-2 security capabilitiesTechnical Report · Published 2 Aug 2017 · ISO/TC 215IEC/TR 80001-2-8:2016WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-8: Application guidance — Guidance on standards for establishing the security capabilities identified in IEC 80001-2-2Technical Report · Published 19 May 2016 · ISO/TC 215ISO/TR 80001-2-7:2015WithdrawnApplication of risk management for IT-networks incorporating medical devices — Application guidance — Part 2-7: Guidance for healthcare delivery organizations (HDOs) on how to self-assess their conformance with IEC 80001-1Technical Report · Published 17 Mar 2015 · ISO/TC 215ISO/TR 80001-2-6:2014WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-6: Application guidance — Guidance for responsibility agreementsTechnical Report · Published 20 Nov 2014 · ISO/TC 215IEC/TR 80001-2-1:2012WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-1: Step by Step Risk Management of Medical IT-Networks; Practical Applications and ExamplesTechnical Report · Published 13 Jul 2012 · ISO/TC 215IEC/TR 80001-2-2:2012WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the communication of medical device security needs, risks and controlsTechnical Report · Published 13 Jul 2012 · ISO/TC 215IEC/TR 80001-2-3:2012WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-3: Guidance for wireless networksTechnical Report · Published 13 Jul 2012 · ISO/TC 215IEC/TR 80001-2-4:2012WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 2-4: General implementation guidance for Healthcare Delivery OrganizationsTechnical Report · Published 3 Dec 2012 · ISO/TC 215IEC 80001-1:2010WithdrawnApplication of risk management for IT-networks incorporating medical devices — Part 1: Roles, responsibilities and activitiesInternational Standard · Published 28 Oct 2010 · ISO/TC 215