The new Medical Devices Regulation (MDR) is a set of regulations that govern the safety and performance requirements of medical devices in the European market
Cerebro has applied for the MDR process along with the CE protocol and has completed all the necessary steps. Our company manufactures all materials used in brain and spinal cord surgery in accordance with the MDR protocol. Therefore, all our products are approved for free circulation and use worldwide.

SPINE SYSTEMS
Thoracalumbar | Anterior Cervical | Interbody Fusion

The Cerebro® Spinal system includes self-tapping polyaxial screws, monoaxial screws, reduction screws and iliac screws. Explore
It has been designed and created with functional and reliable application sets that facilitate the
application, considering that it provides comfort both in surgical practice and in the life comfort
of patients.
The parts that make up the system are made of intracorporeal compatible Titanium alloy (Ti6Al4V-ELI) and MR compatible peek material (EVONIK), which is a body compatible thermoplastic solution for in-vivo applications and does not create any artifacts.
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