Guide - ANVISA Registration 81194869005

Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81194869005 and manufactured by DILON TECHNOLOGIES INC. The registration is held by PROEXI COMERCIO, EXPORTACAO E IMPORTACAO DE PRODUTOS MEDICOS E HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DPS INDUSTRIA, DISTRIBUICAO, COMERCIO, IMPORTACAO E EXPORTACAO LTDA, CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA., 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.