TREPONEMA PALLIDUM - ANVISA Registration 80002670128

Access comprehensive regulatory information for TREPONEMA PALLIDUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80002670128 and manufactured by RENYLAB QUÍMICA E FARMACÊUTICA LTDA. The registration is held by RENYLAB QUÍMICA E FARMACÊUTICA LTDA with validity until Sep 23, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including WAMA PRODUTOS PARA LABORATORIO LTDA, EUROIMMUN 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.