Dear Member,

In the letter dated 08.10.2025 and numbered 12739, sent to our Chamber from the Union of Chambers and Commodity Exchanges of Türkiye,

It has been announced that the European Commission has launched a consultation process on Regulation (EU) No. 2017/745 on Medical Devices (MDR) and Regulation (EU) No. 2017/746 on In Vitro Diagnostic Medical Devices (IVDR), which were adopted in 2017.

In the letter, it was stated that the Commission should carry out an assessment of the consultation process by May 2027, in order to ensure a smooth transition to the new rules under the MDR and IVDR Regulations, within the framework of the relevant articles of the Regulations.

The article continues by stating that detailed information regarding the feedback process can be accessed through the link provided in the article and that comments can be submitted until October 6, 2025.

Best regards.