Regenerative Membranes - ANVISA Registration 80255120001

Access comprehensive regulatory information for Regenerative Membranes in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80255120001 and manufactured by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA. The registration is held by BIONEXT PRODUTOS BIOTECNOLOGICOS LTDA with validity until Jan 09, 2036.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including INTEGRA LIFESCIENCES CORPORATION, INTEGRA LIFESCIENCES CORPORATION (PRINCETON), 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.