Bone Distractor - ANVISA Registration 80455630118

Access comprehensive regulatory information for Bone Distractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80455630118 and manufactured by TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP. The registration is held by TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS IMP. E EXP. LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 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.