IMMUNOHEMATOLOGY - RARE SERA FOR CONVENTIONAL METHODOLOGY - ANVISA Registration 80134860265

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 80134860265 and manufactured by MEDION GRIFOLS DIAGNOSTICS AG. The registration is held by GRIFOLS BRASIL LTDA with validity until Sep 02, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.