IMMUNOHEMATOLOGY - RARE SERA FOR CONVENTIONAL METHODOLOGY - ANVISA Registration 80134860316

Access comprehensive regulatory information for IMMUNOHEMATOLOGY - RARE SERA FOR CONVENTIONAL METHODOLOGY in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80134860316 and manufactured by MEDION DIAGNOSTICS GRIFOLS AG. The registration is held by GRIFOLS BRASIL LTDA with validity until Jun 30, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MEDION GRIFOLS DIAGNOSTICS AG, MEDION DIAGNOSTICS GRIFOLS AG, 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.