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Register as a manufacturer to sell medical devices

Register as a manufacturer to sell medical devices
December 9, 2020 SueCarr

From 1 January onwards the following devices will need to be registered with the MHRA under existing arrangements:

  • Class I medical devices
  • IVDs
  • Custom made devices

All other classes of device placed on the GB market will require registration with the MHRA subject to grace periods over the following 12 months, depending on the class of devices and as detailed on the MHRA website.

Registration requirements under those regulations differ for Northern Ireland.

 

Find out more here:

Register as a manufacturer to sell medical devices

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