Tubular Mesh - ANVISA Registration 80018110077

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 80018110077 and manufactured by DILEPE INDUSTRIA COMERCIO DE MAT ORTOPEDICOS LTDA. The registration is held by DILEPÉ INDÚSTRIA E COMÉRCIO DE MATERIAIS ORTOPÉDICOS 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.