The Medical Devices Regulation (MDR) is fully applicable since May 26, 2021.
To prevent market disruptions and give manufacturers enough time to certify their medical devices under the new Regulation, medical devices certified under the previous Directives can be subject to a “legacy period” (grace period).
Register and watch our new webinar to get an insight on:
- Legacy period for medical devices certified under previous EU Directives
- EU: New legacy extension periods
- Extra conditions for manufacturers
- UK: Recognition of extended CE Certificates
- Switzerland: Recognition of extended CE Certificates
- How can Obelis help you?
- Q&A
Interested in watching the recording?
Watch it now!