Response Stimulator for Diagnosis - ANVISA Registration 80117580341

Access comprehensive regulatory information for Response Stimulator for Diagnosis in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80117580341 and manufactured by TONICA ELEKTRONIK A/S. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Apr 06, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.