Guide - ANVISA Registration 81050760137

Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81050760137 and manufactured by ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD.. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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.