Tube Sealer - ANVISA Registration 10154459025

Access comprehensive regulatory information for Tube Sealer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10154459025 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL 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 DELCON S.R.L., OLIDEF CZ IND E COM DE APARELHOS HOSPITALARES 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.