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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 13 – Procedure for custom-made devices

For custom-made devices, the manufacturer or its authorised representative shall draw up a statement containing all of the following information:
the name and address of the manufacturer, and of all manufacturing sites,
if applicable, the name and address of the authorised representative,
data allowing identification of the device in question,
a statement that the device is intended for exclusive use by a particular patient or user, identified by name, an acronym or a numerical code,
the name of the person who made out the prescription and who is authorised by national law by virtue of their professional qualifications to do so, and, where applicable, the name of the health institution concerned,
the specific characteristics of the product as indicated by the prescription,
a statement that the device in question conforms to the general safety and performance requirements set out in
Annex I
⁠
and, where applicable, indicating which general safety and performance requirements have not been fully met, together with the grounds,
where applicable, an indication that the device contains or incorporates a medicinal substance, including a human blood or plasma derivative, or tissues or cells of human origin, or of animal origin as referred to in Regulation (EU) No 722/2012.
The manufacturer shall undertake to keep available for the competent national authorities documentation that indicates its manufacturing site or sites and allows an understanding to be formed of the design, manufacture and performance of the device, including the expected performance, so as to allow assessment of conformity with the requirements of this Regulation.
The manufacturer shall take all the measures necessary to ensure that the manufacturing process produces devices which are manufactured in accordance with the documentation referred to in Section 2.
The statement referred to in the introductory part of Section 1 shall be kept for a period of at least 10 years after the device has been placed on the market. In the case of implantable devices, the period shall be at least 15 years. Section 8 of
Annex IX
⁠
shall apply.
The manufacturer shall review and document experience gained in the post-production phase, including from PMCF as referred to in Part B of
Annex XIV
⁠
, and implement appropriate means to apply any necessary corrective action, In that context, it shall report in accordance with
Article 87(1)
⁠
to the competent authorities any serious incidents or field safety corrective actions or both as soon as it learns of them.
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