CULTURE MEDIA AND DEVICES FOR ANAEROBE RESEARCH - ANVISA Registration 80254180292

Access comprehensive regulatory information for CULTURE MEDIA AND DEVICES FOR ANAEROBE RESEARCH in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80254180292 and manufactured by REMEL INC.. The registration is held by PHADIA DIAGNOSTICOS 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, 5 companies making the same product including BECTON DICKINSON AND COMPANY, ZHEJIANG QUARK BIOTECHNOLOGY CO., LTD., 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.