Post-Surgical Mesh - ANVISA Registration 80674930018

Access comprehensive regulatory information for Post-Surgical Mesh in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80674930018 and manufactured by TYTEX A/S. The registration is held by GCA BRASIL IMPORTACAO E EXPORTACAO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including BOA FORMA CONFECÇÕES LTDA, Plie Confecções 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.