The same team and the same mandate, extended to the Turkish market.
Medical devices sold in Türkiye must be registered in ÜTS, the Turkish national device database, and manufacturers established abroad must appoint a representative in Türkiye.
For a manufacturer outside the EU this normally means two separate appointments: one authorised representative in the European Union and another in Türkiye. Because Medex is established in Türkiye and acts as an EU authorised representative under the Customs Union arrangement, a single mandate covers both markets.
We handle ÜTS registration, product registrations and ongoing representation for the Turkish market — under the same contract, with the same people.
For most manufacturers already entering the EU, adding a market of over 80 million people costs very little extra.
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