Ecobone Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit - EUDAMED Registration 08681781334427

Access comprehensive regulatory information for Ecobone Bone Cement Vertebroplasty, Percutaneous Posterior, Vertebroplasty Kit in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 08681781334427 and manufactured by Bonegraft Biomaterials Co. in Turkey.

This page provides complete registration details including trade name (Ecobone), manufacturer information, competent authority (Turkish Medicine and Medical Devices Agency), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.