The Dental Sector's Reliable Regulatory and Medical Device Registration Partner
Dental UTS Consultancy Services is a professional solution partner that manages medical device registration and regulatory compliance processes for manufacturers, importers, master distributors and dental warehouses at every level of the medical and dental sector.
We are by your side with a results-oriented, professional structure that is fully compliant with the current legislation on the Product Tracking System (ÜTS) covering healthcare products. We take on all ÜTS supply-consumption notifications and operational procedures, from the TİTCK certification process of your products to reaching the end user.
For dental warehouses, clinics, importers and domestic manufacturers, we make complex bureaucratic processes "understandable and manageable". From ÜTS medical device registrations to State Supply Office (DMO) Health Market catalogue applications, we lighten your operational load across a wide range.
Our goal is not merely to provide a consultancy service; it is to be a strategic business partner that prevents your business from suffering regulatory-driven commercial losses, accelerates your processes and contributes to your growth.
We register your company's medical devices and consumables in the system, track document updates and manage regulatory compliance processes.
Starting from production/import notifications, we carry out all supply-consumption transactions between companies, dentists and clinics, as well as unique device identification (UDI) processes, flawlessly.
We professionally handle your products' entry into the DMO e-sales portal, technical specification compliance and the preparation of tender files.
From the import stage onward, we make the legal notifications of your products and carry out regulatory compliance checks, protecting your company against administrative risks.
We provide hands-on regulatory training for dentists and laboratories on ÜTS notifications, which have become a legal obligation, and set up systems that protect your organisation from administrative fines.
We carry out actor registration and the required registration processes under the European Medical Device Database (EUDAMED) on behalf of your company.
To be the first solution centre that comes to mind when regulation and digital integration are mentioned in the Turkish dental sector; and to enable companies to trade safely on a legal footing and to global standards.
To manage our clients' ÜTS and DMO processes with a "Zero Error" principle, to ensure the fastest compliance with changing regulations, and to allow businesses to focus on their core activities of sales and service.