Equipment and Tube Welder - ANVISA Registration 10154459024

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 10154459024 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 companies making the same product including GENESIS BPS, GENESISBPS, 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.