Tubular Mesh - ANVISA Registration 80028209005

Access comprehensive regulatory information for Tubular 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 80028209005 and manufactured by GIMED CONFECÇÕES HOSPITALARES LTDA. The registration is held by GIMED CONFECÇÕES HOSPITALARES LTDA with validity until currently active (VIGENTE).

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 SANTRIC INDUSTRIA E COMERCIO LTDA EPP, POLAR FIX INDUSTRIA E COMERCIO DE PRODUTOS HOSPITALARES 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.