Reusable endoscopic, bipolar electrosurgical electrode - ANVISA Registration 80943610237

Access comprehensive regulatory information for Reusable endoscopic, bipolar electrosurgical electrode in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80943610237 and manufactured by manufacturer not specified. The registration is held by MINDRAY DO BRASIL COMÉRCIO E DISTRIBUIÇÃO DE EQUIPAMENTOS MÉDICOS LTDA. with validity until Feb 24, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including ENDOMED SRLS, Nexxmed Equipamentos Ltda, and 2 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.