MYCOPLASMA - ANVISA Registration 80102513471

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 80102513471 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jul 07, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including EUROIMMUN AG, BIO-RAD, 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.