The extension of the MDR transition period for legacy devices has allowed manufacturers who met the required conditions to benefit from additional time to bring their devices into compliance with the new regulation.

Although the deadlines may seem distant, the necessary activities should not be underestimated. In this webinar, we will revisit several aspects related to the management of this transition period, to explain which key points manufacturers need to take into account and what the role and challenges of a Notified Body like BSI might be in this context. We will also take a look at the requirements for maintaining regulatory compliance through the surveillance of legacy devices