Authorised Representative

A representative located within the EU or target region appointed by an overseas manufacturer to handle regulatory obligations.

Non-EU manufacturers exporting medical devices to the European Economic Area must designate an Authorised Representative (EC REP). The representative acts as the contact point for local Competent Authority inquiries and verifies EUDAMED submission completeness.

Explore the data behind the terms

HaRi brings the FDA, MHRA, EUDAMED, Health Canada and TGA registers into one search: devices, manufacturers, product codes and safety events, all cross-referenced and free to explore.