CLOSTRIDIUM TETANI - ANVISA Registration 80105220287

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 80105220287 and manufactured by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA with validity until Sep 01, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DIA.PRO DIAGNOSTIC BIOPROBES SRL, INSTITUT VIRION\SERION GMBH, 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.