We manage your Product Tracking System (ÜTS) medical device registrations, supply-consumption notifications and DMO Health Market catalogue processes with a professional system. We take over your device and dental consumable registration processes with a zero-error principle.
For dental warehouses, clinics, importers and manufacturers, we turn the complex TİTCK and ÜTS regulatory processes into a clear road map.
In the dental sector, we professionally manage the entire ÜTS medical device registration and State Supply Office (DMO) journey — from customs clearance of a product all the way to its use on the patient. While you focus on your sales and patients, we carry the bureaucratic load in the background.
All the Solutions the Dental and Medical Sector Needs
We track instant changes in the Medical Device Regulation (MDR) and ÜTS legislation, and manage your ÜTS company registration and document updates.
We complete the document registrations and technical file reviews of the devices you import or manufacture in full, accelerating your market entry.
In State Supply Office (DMO) processes, we handle Health Market applications, product matching and order management on your behalf and manage your public-sector sales.
For dental clinics and hospitals, we systematise stock tracking, supply-consumption notifications and consumable usage processes, preventing leaks.
For ÜTS processes that have become a legal obligation under TİTCK legislation, we provide professional compliance training that protects your organisation from administrative fines.
In European Medical Device Database (EUDAMED) processes, we fully manage actor registration, UDI/device registration and module compliance on behalf of your company.
We review your company's current situation and chart the fastest legal route suited to your product range and goals.
We complete your products' ÜTS registrations, DMO catalogue applications and technical file preparations in full.
We track all your notification processes and take instant action on regulatory updates, ensuring operational continuity.
Latest Developments in ÜTS and TİTCK Legislation
Petitions submitted to the Provincial Health Directorate for devices that cannot be registered in ÜTS are no longer valid. If a medical device without an ÜTS registration (except products manufactured before 2007) is detected during routine audits, it will be recorded directly as non-compliance.
Contact UsUse of the EUDAMED database system became mandatory on 28 May 2026. It is important to plan the required processes, starting with actor registration, without losing time.
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