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MDR Flowchart Explains When Legacy Devices Can Benefit From Extended Timelines

 
• By Amanda Maxwell

Are you uncertain whether your medtech products can benefit from transition period extensions that feature in the March 2023 amending Regulation to the MDR? The latest European Commission document offers help.

Algorithm, flowchart. 3D rendering isolated on white background

The European Commission has published a document to help manufacturers and other relevant medtech sector actors decide whether a device can benefit from the extended transitional period brought in under the recent amending regulation to Medical Device Regulation and under what conditions. (Also see "MDR Amending Regulation Officially Published And Already In Force" - Medtech Insight, 20 March, 2023.)

The document is available here:

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