BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 80686360208

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 80686360208 and manufactured by KASIOS SAS. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA with validity until Feb 11, 2029.

This page provides complete technical specifications for 2 related devices, 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.