BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 80255120002

Access comprehensive regulatory information for BONE GRAFT AND ASSOCIATED DEVICES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80255120002 and manufactured by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA. The registration is held by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA with validity until Aug 05, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including GEISTLICH PHARMA AG, M3 Health Indústria e Comércio de Produtos Médicos, Odontológicos e Correlatos S.A., 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.