Medical Device Regulation MDR 2017 745 Mindmap EN
Medical Device Regulation MDR 2017 745 Mindmap EN
Medical Device Regulation MDR 2017 745 Mindmap EN
Article 2: Definitions
Chapter I
Article 123: Entry into force and date of application Article 3: Amendment of certain definitions
Scope and Definitions (1-4)
Article 122: Repeal Article 4: Regulatory status of products
Chapter X
Article 118: Amendments to regulations (EC) No 178/2002 General Article 7: Claims
Final provisions (114-123)
Article 117: Amendments to directive 2001/83(/EC Article 8: Use of harmonised standards
Article 116: Separate delegated acts for different delgated powers Article 9: Common specifications
Article 115: Exercise of the delegation Article 10: General obligations of the manufacturer
Article 106: Provision of scientific, technical an clinical opinion and Article 20: CE marking of conformity
advice
Article 91: Implementing acts Article 36: Requirements relating to notified bodies
Chapter VII
Article 90: Analysis of vigilance data Post-market surveillance, vigilance and market Article 37: Subsidiaries and subcontracting
Section 2: surveillance (83-100)
Article 89: Analysis of serious incidents and field safety corrective Vigilance Article 38: Application by conformity assessment bodies for
actions designation
Article 87: Reporting of serious incidents and field safety corrective Article 40: Nomination of experts for joint assessment of
actions applications for notification
Article 86: Periodic safety update report Article 41: Language requirements
Article 85: Post-market surveillance report Section 1: Article 42: Designation and notification procedure
Post market surveillance Chapter IV
Article 43: Identification number and list of notified bodies
Article 84: Post-market surveillance plan Notified bodies (35-50)
Article 44: Monitoring and re-assessment of notified bodies
Article 83: Post-market surveillance system of the manufacturer
Article 72: Conduct of a clinical investigation Chapter VI Article 55: Mechanism for scrutiny of conformity assessments of
certain class III and class IIb devices
Clinical evaluation and clinical investigations (61-82) Section 2
Article 71: Assessment by member states Conformity assessment
Article 56: Certificates of conformity
Article 70: Application for clinical investigations
Article 57: Electronic system on notified bodies and on certificates of
Article 69: Damage compensation conformity
Article 68: Clinical investigations in emergency situations Article 58: Voluntary change of notified body
Article 67: Additional national measures Article 59: Derogation from the conformity assessment procedures
Article 66: Clinical investigations on pregnant or breastfeeding Article 60: Certificate of free sale
women