Vacuum Regulator - ANVISA Registration 80239100005

Access comprehensive regulatory information for Vacuum Regulator in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80239100005 and manufactured by GENTEC (SHANGHAI) CORPORATION. The registration is held by BIOCATH COMÉRCIO DE PRODUTOS HOSPITALARES LTDA 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 JG MORIYA REPRESENTAÇÃO IMPORTADORA EXPORTADORA COMERCIAL LTDA, Technologie Medicale, 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.