Milestone 4 of 6 Selling medical devices in both GB and Northern Ireland

Step 4: Appoint your representatives

Dual-market access may require two separate representatives:

  • UK Responsible Person (UKRP): Required for non-UK manufacturers placing devices on the GB market. Must be UK-established.
  • EU Authorised Representative: Required for non-EU/non-NI manufacturers placing devices on the NI market. Must be established in the EU or Northern Ireland.

If you are a Great Britain-based manufacturer selling into NI, you need an authorised representative based in the EU or NI but not a UKRP. A manufacturer based in NI does not need one for the NI market. If you are an EU manufacturer selling into GB, you need a UKRP but not an EU Authorised Representative.