Plasma Processing Set - ANVISA Registration 10154450215

Access comprehensive regulatory information for Plasma Processing Set in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10154450215 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until Aug 19, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including FRESENIUS KABI AG, VIVOSTAT A/S, 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.