UK – MHRA shares guidance on need to review registration of medical devices

MHRA has told medical device manufacturers to review their registration information “frequently” to ensure it is up to date. The agency provided the advice in an update to its guidance on registering medical devices.

Companies are legally required to tell MHRA about any changes in their registrations. MHRA has set up an “update registered devices and products functionality” companies can use to update data fields that were not previously populated. MHRA is urging companies to use the function to add UDI-DIs given their importance for patient safety. There is no fee for using the function…