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Full text of EU MDR (Medical Device Regulation)
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EU MDR Table of Contents
Chapter 1 (Art. 1 – 4)
Scope and definitions
Chapter 2 (Art. 5 – 24)
Making available on the market and putting into service of devices, obligations of economic operators, reprocessing, CE marking, free movement
Chapter 3 (Art. 25 – 34)
Identification and traceability of devices, registration of devices and of economic operators, summary of safety and clinical performance, European database on medical devices
Chapter 4 (Art. 35 – 50)
Notified bodies
Chapter 5 (Art. 51 – 60)
Classification and conformity assessment
Section 1 (Art. 51)
Classification
Section 2 (Art. 52 – 60)
Conformity assessment
Chapter 6 (Art. 61 – 82)
Clinical evaluation and clinical investigations
Chapter 7 (Art. 83 – 100)
Post-market surveillance, vigilance and market surveillance
Section 1 (Art. 83 – 86)
Post-market surveillance
Section 2 (Art. 87 – 92)
Vigilance
Section 3 (Art. 93 – 100)
Market surveillance
Chapter 8 (Art. 101 – 108)
Cooperation between member states, medical device coordination group, expert laboratories, expert panels and device registers
Chapter 9 (Art. 109 – 113)
Confidentiality, data protection, funding and penalties
Chapter 10 (Art. 114 – 123)
Final provisions
(Anx. 1 – 17)
Annexes
Source EUR-Lex:
https://eur-lex.europa.eu/
EU MDR
Chapter 7
Section 3
Section 3 –
Market surveillance
Article 93
–
Market surveillance activities
Article 94
–
Evaluation of devices suspected of presenting an unacceptable risk or other non-compliance
Article 95
–
Procedure for dealing with devices presenting an unacceptable risk to health and safety
Article 96
–
Procedure for evaluating national measures at Union level
Article 97
–
Other non-compliance
Article 98
–
Preventive health protection measures
Article 99
–
Good administrative practice
Article 100
–
Electronic system on market surveillance
« Chapter 7 – Post-market ...
Article 93 – Market surv... »
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