What is the webinar about?
After a summary of the device types covered under Annex XVI (EU) 2017/745 and Common Specification 2022/23/48, the webinar will clarify the different transition provisions for these types of devices, the routes to conformity including CECP requirements and differences in classification for certain active Annex XVI devices.
What will participants gain?
Join the webinar to:
- Explore the types of devices covered under Annex XVI and the transitions provisions for these types of devices.
- Understand the route to conformity including CECP requirements and differences in classification for certain active Annex XVI devices.
Who should attend?
Anyone involved in certifying devices without an intended medical purpose under the MDR.
Register for the webinar on Tuesday 17 April 2024. Please note, there is only one session for this webinar:
16.00 - 17.00 BST - Register here
Speakers
Neill
Bannister
Global Head of General Devices, Regulatory Services, BSI
Dr. Nick
Trilokekar
Technical Team Manager, General Devices, Regulatory Services, BSI
Email: medicaldevices@bsigroup.com
Phone: +44 3450809000
