Post-Surgical Mesh - ANVISA Registration 82217800019

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 82217800019 and manufactured by Plie Confecções Ltda. The registration is held by Plie Confecções 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 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.