Equipment and Tube Welder - ANVISA Registration 80832339008

Access comprehensive regulatory information for Equipment and Tube Welder in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80832339008 and manufactured by GENESIS BPS. The registration is held by COMERCIAL BRASIL COMERCIO, IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICO-HOSPITALARES LTDA-EPP 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 GENESISBPS, 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.