Suspenders (scrotal, hernia and others) - ANVISA Registration 80758210041

Access comprehensive regulatory information for Suspenders (scrotal, hernia and others) in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80758210041 and manufactured by HIDROLIGHT DO BRASIL S.A.. The registration is held by HIDROLIGHT DO BRASIL S.A. 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 HANESBRANDS BRASIL TEXTIL LTDA, Famara Brasil Indústria e Comércio Ltda - EPP, 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.