This page lists the opinions provided under the Clinical Evaluation Consultation Procedure (CECP, see Article 54 of Regulation (EU) 2017/745) by each thematic expert panel in the field of medical devices.
The Commission draws up an annual overview of devices which have been subject to the CECP.
- Annual overview of devices subject to the CECP (July 2022- June 2023)
- Annual overview of devices subject to the CECP (April 2021- June 2022)
1. Orthopaedics, traumatology, rehabilitation, rheumatology
2. Circulatory system
- 10.01.2025, NB2265, CECP-EMA/EX/0000236104
- 11.11.2022, NB0123, CECP-2022-000235
- 05.07.2022, NB0344, CECP-2022-000225
- 27.06.2022, NB0344, CECP-2022-000216
- 23.05.2022, NB0344, CECP-2022-000213
- 07.12.2021, NB0344, CECP-2021-000207
3. Neurology
4. Respiratory system, anaesthesiology, intensive care
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5. Endocrinology and diabetes
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6. General and plastic surgery and dentistry
- 10.06.2024, NB2797 CECP- EMA/EX/0000175268
- 06.10.2022, NB2797, CECP-2022-000227
- 15.06.2021, NB0483, CECP-2021-000201
7. Obstetrics and gynaecology, including reproductive medicine
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8. Gastroenterology and hepatology
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9. Nephrology and urology
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10. Ophthalmology
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Details of the notified bodies may be found here.