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EU MDR
Dynamic EU MDR 2017/745 Full Text
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
Chapter 6 (Art. 61 – 82) Clinical evaluation and clinical investigations
Chapter 7 (Art. 83 – 100) Post-market surveillance, vigilance and 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
Annexes
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Annexes

Annex 12 – Certificates issued by a notified body

Chapter 1

GENERAL REQUIREMENTS
Certificates shall be drawn up in one of the official languages of the Union.
Each certificate shall refer to only one conformity assessment procedure.
Certificates shall only be issued to one manufacturer. The name and address of the manufacturer included in the certificate shall be the same as that registered in the electronic system referred to in
Article 30
⁠
.
The scope of the certificates shall unambiguously identify the device or devices covered:
EU technical documentation assessment certificates, EU type-examination certificates and EU product verification certificates shall include a clear identification, including the name, model and type, of the device or devices, the intended purpose, as included by the manufacturer in the instructions for use and in relation to which the device has been assessed in the conformity assessment procedure, risk classification and the Basic UDI-DI as referred to in
Article 27(6)
⁠
;
EU quality management system certificates and EU quality assurance certificates shall include the identification of the devices or groups of devices, the risk classification, and, for class IIb devices, the intended purpose.
The notified body shall be able to demonstrate on request, which (individual) devices are covered by the certificate. The notified body shall set up a system that enables the determination of the devices, including their classification, covered by the certificate.
Certificates shall contain, if applicable, a note that, for the placing on the market of the device or devices it covers, another certificate issued in accordance with this Regulation is required.
EU quality management system certificates and EU quality assurance certificates for class I devices for which the involvement of a notified body is required pursuant to
Article 52(7)
⁠
shall include a statement that the audit by the notified body of the quality management system was limited to the aspects required under that paragraph.
Where a certificate is supplemented, modified or re-issued, the new certificate shall contain a reference to the preceding certificate and its date of issue with identification of the changes.
Chapter 2
MINIMUM CONTENT OF THE CERTIFICATES
name, address and identification number of the notified body;
name and address of the manufacturer and, if applicable, of the authorised representative;
unique number identifying the certificate;
if already issued, the SRN of the manufacturer referred to in to
Article 31(2)
⁠
;
date of issue;
date of expiry;
data needed for the unambiguous identification of the device or devices where applicable as specified in Section 4 of Part I;
if applicable, reference to any previous certificate as specified in Section 8 of Chapter I;
reference to this Regulation and the relevant Annex in accordance with which the conformity assessment has been carried out;
examinations and tests performed, e.g. reference to relevant CS, harmonised standards, test reports and audit report(s);
if applicable, reference to the relevant parts of the technical documentation or other certificates required for the placing on the market of the device or devices covered;
if applicable, information about the surveillance by the notified body;
conclusions of the notified body’s conformity assessment with regard to the relevant Annex;
conditions for or limitations to the validity of the certificate;
legally binding signature of the notified body in accordance with the applicable national law.
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