CLOSTRIDIUM TETANI - ANVISA Registration 10338930328

Access comprehensive regulatory information for CLOSTRIDIUM TETANI in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10338930328 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Jan 13, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA, DIA.PRO DIAGNOSTIC BIOPROBES SRL, 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.