BONE GRAFT AND ASSOCIATED DEVICES - ANVISA Registration 81684340024

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 81684340024 and manufactured by M3 Health Indústria e Comércio de Produtos Médicos, Odontológicos e Correlatos S.A.. The registration is held by M3 HEALTH INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS, ODONTOLOGICOS E CORRELATOS S.A. with validity until Jun 09, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including GEISTLICH PHARMA AG, BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA, 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.