TREPONEMA PALLIDUM - ANVISA Registration 80537410137

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 80537410137 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD. The registration is held by CELER BIOTECNOLOGIA S/A with validity until Jun 09, 2035.

This page provides complete technical specifications for 2 related devices, 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.