Professional Solutions in Medical Device Registration, Supply-Consumption Notifications and DMO Processes
We carry out all ÜTS product registration and ÜTS company registration processes required to place medical devices, consumables and cosmetic products on the market in full compliance with the legislation. We do not just register; we monitor document validity periods, certificate updates and TİTCK announcements on your behalf in real time, ensuring you always remain active on the Product Tracking System.
We manage the stock traffic on ÜTS for all stakeholders, from manufacturers and importers to the smallest dental clinics.
We prepare all the technical infrastructure you need to exist in public sales channels. In State Supply Office (DMO) e-sales portal and Health Market applications, we ensure your products are entered in line with technical specifications, and provide professional support for DMO catalogue applications, the complete preparation of your tender files and process monitoring.
We keep all your company's processes — from the import stage to the end user — ready for legal audits at all times. We analyse Medical Device Regulation (MDR, IVDR, etc.) updates on your behalf, and take on risk management and technical documentation preparation so your company does not face administrative sanctions.
For ÜTS notification processes that have become a legal obligation under TİTCK legislation, we organise comprehensive corporate ÜTS training for your clinics and laboratories.
The European Medical Device Database (EUDAMED) is the central traceability system for medical devices under MDR/IVDR. Use of the first four modules became mandatory as of 28 May 2026.