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GMDN Agency welcomes UK-wide Medical Device Information System

  • Jan 8, 2021
  • 1 min read


From 1st January 2021 all medical devices placed on the market must be registered by their manufacturers with the MHRA as part of a UK-wide Medical Device Information System (MDIS).


This will provide a national resource for hospitals, patients and suppliers to identify and manage the medical technology they use.



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