Blood bank centrifuge - ANVISA Registration 10154450157

Access comprehensive regulatory information for Blood bank centrifuge in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10154450157 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, 1 companies making the same product including QINGDAO HAIER BIOMEDICAL CO., LTD., and 1 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.