Medical device registration is handled by TITUBB, the Turkish National Database for Medical Devices. CLASSIFICATION:
Classification follows the EU model of risk-based classification into Classes I, IIa, IIb, III, and IV. TIMEFRAME:
The approval process takes about 3-5 months. AUTHORIZED REPRESENTATIVE:
An authorized representative is required. ADDITIONAL INFORMATION:
Translation and legalization of all documents should be carried out by a Turkish company.
Last updated on March 17 2015.
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For more information on registration in Turkey, check out the following articles on our blog: Country at a Glance: Turkey