Electroshock Device - ANVISA Registration 80022370015

Access comprehensive regulatory information for Electroshock Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80022370015 and manufactured by SWITECH MEDICAL AG. The registration is held by TRT ENGENHARIA E EQUIPAMENTOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.