MYCOPLASMA - ANVISA Registration 81148560039

Access comprehensive regulatory information for MYCOPLASMA in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81148560039 and manufactured by manufacturer not specified. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Dec 19, 2026.

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 BIO-RAD, NOVATEC IMMUNDIAGNOSTICA GMBH TECHNOLOGIE & WALDPARK, 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.