Plasma Extractor - ANVISA Registration 80867150187

Access comprehensive regulatory information for Plasma Extractor in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80867150187 and manufactured by OK BIOTECH CO., LTD.. The registration is held by BIOMOLECULAR TECHNOLOGY COMÉRCIO, IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO DE MATERIAIS MÉDICOS E LABORATORIAIS LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including FANEM LTDA, TERUMO CORPORATION, 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.