emendrix

Art. 17

Medical Devices Regulation · 32017R0745 · every event for this act · on EUR-Lex

Single-use devices and their reprocessing

1 change recorded across 1 event, newest first.

in force 2020-04-24 DEFERRED+14 −14

Amended by Regulation (EU) 2020/561 32020R0561

applies from: 2021-05-26

dates added to the text: 2021-05-26 · dates removed: 2020-05-26

The two dates in paragraph 5, which set the deadline for adopting common specifications and the fallback trigger date, moved from 26 May 2020 to 26 May 2021.

The date in paragraph 6, marking the cutoff for devices placed on the market under Directive 93/42/EEC to be eligible for reprocessing, likewise moved from 26 May 2020 to 26 May 2021.

Cited: Art. 17, v1 · Art. 17, v2

text before / after

02017R0745-2017050502017R0745-20200424

Article 17 Single-use devices and their reprocessing 1. Reprocessing and further use of single-use devices may only take place where permitted by national law and only in accordance with this Article. 2. Any natural or legal person who reprocesses a single-use device to … 353 unchanged words … the external reprocessor complies with the requirements referred to in points (a) and (b) of paragraph 3. 5. The Commission shall adopt, in accordance with Article 9(1), the necessary CS referred to in point (b) of paragraph 3 by 26 May 2020. 2021. Those CS shall be consistent with the latest scientific evidence and shall address the application of the general requirements on safety and performance laid down in in this Regulation. In the event that those CS are not adopted by 26 May 2020, 2021, reprocessing shall be performed in accordance with any relevant harmonised standards and national provisions that cover the aspects outlined in point (b) of paragraph 3. Compliance with CS or, in the absence of CS, with any relevant harmonised standards and national provisions, shall be certified by a notified body. 6. Only single-use devices that have been placed on the market in accordance with this Regulation, or prior to 26 May 2020 2021 in accordance with Directive 93/42/EEC, may be reprocessed. 7. Only reprocessing of single-use devices that is considered safe according to the latest scientific evidence may be carried out. 8. The name and address of the legal or natural person referred to in paragraph 2 and the other relevant information referred to in Section 23 of Annex I shall be indicated on the label and, where applicable, in the instructions for use of the reprocessed device. The name and address of the manufacturer of the original single-use device shall no longer appear on the label, but shall be mentioned in the instructions for use of the reprocessed device. 9. A Member State that permits reprocessing of single-use devices may maintain or introduce national provisions that are stricter than those laid down in this Regulation and which restrict or prohibit, within its territory, the following: (a) the reprocessing of single-use devices and the transfer of single-use devices to another Member State or to a third country with a view to their reprocessing; (b) the making available or further use of reprocessed single-use devices. Member States shall notify the Commission and the other Member States of those national provisions. The Commission shall make such information publicly available. 10. The Commission shall by 27 May 2024 draw up a report on the operation of this Article and submit it to the European Parliament and to the Council. On the basis of that report, the Commission shall, if appropriate, make proposals for amendments to this Regulation.