Kaulmed Vertebroplasty, Percutaneous Posterior, Vertebroplasty Bone Interference Set, Metal-Plastic - EUDAMED Registration 08681781335349

Access comprehensive regulatory information for Kaulmed Vertebroplasty, Percutaneous Posterior, Vertebroplasty Bone Interference Set, Metal-Plastic 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 08681781335349 and manufactured by Bonegraft Biomaterials Co. in Turkey.

This page provides complete registration details including trade name (Kaulmed), 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.