Probes - ANVISA Registration 81263810008

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81263810008 and manufactured by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA. The registration is held by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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.