Kit for Blood Recovery Machine - ANVISA Registration 10154450181

Access comprehensive regulatory information for Kit for Blood Recovery Machine in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10154450181 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS HEMOCARE BRASIL LTDA. with validity until Nov 27, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including FRESENIUS KABI AG, TERUMO BCT INC, 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.