Bone Distractor - ANVISA Registration 80254350029

Access comprehensive regulatory information for Bone Distractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254350029 and manufactured by ALLIED TITANIUM LTDA. The registration is held by ALLIED TITANIUM LTDA with validity until Apr 16, 2028.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ENGIMPLAN ENGENHARIA DE IMPLANTE IND E COM LTDA, TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.