Medical Device UTS Procedures: Quality Consulting and Regulatory Compliance

Medical devices play a critical role in the healthcare industry, and the production, import, export and sale of these devices are highly regulated processes. In Turkey, medical devices are tracked from the production line to the end user through the Product Tracking System (UTS). As Kalitetürk Consulting , we offer you professional consulting services in this process.

What is Product Tracking System (UTS)?

ÜTS is a project developed to ensure individual product tracking of medical devices manufactured or imported in Turkey from the production line to where they are sold and used. Thanks to this system, it is possible to track medical devices all the way to the end user and ensure their security.

Frequently Asked Questions

What is the purpose of UTS?

The main purpose of ÜTS is to monitor the process from the production line of medical devices to the end user and to ensure the safety of these products.

Who should register for ÜTS?

Medical device manufacturers, importers and exporters must register with ÜTS.

How are UTS transactions carried out?

ÜTS transactions must be carried out in accordance with a specific procedure and legislation. Getting professional consultancy during this process ensures that the transactions are completed quickly and without errors .