TREPONEMA PALLIDUM - ANVISA Registration 10303460223

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 10303460223 and manufactured by manufacturer not specified. The registration is held by IN VITRO DIAGNOSTICA LTDA with validity until Aug 13, 2027.

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 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.