Sling - ANVISA Registration 80758210019

Access comprehensive regulatory information for Sling in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80758210019 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 similar products found using AI-powered semantic search, 5 companies making the same product including HIDROLIGHT DO BRASIL S.A., ATLET BRASIL 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.