BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 81326140001

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 81326140001 and manufactured by REGENER INDUSTRIA E COMERCIO DE BIOMATERIAIS LTDA. The registration is held by REGENER INDUSTRIA E COMERCIO DE BIOMATERIAIS LTDA with validity until Feb 26, 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 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.