Bipolar Forceps - ANVISA Registration 80003890141

Access comprehensive regulatory information for Bipolar Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80003890141 and manufactured by manufacturer not specified. The registration is held by CANADA CENTRAL DE NEGOCIOS DO BRASIL LTDA with validity until Oct 13, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including euro parts brasil industria e comercio de instrumental cirurgico ltda, TECNO INSTRUMENTS (PVT) LTD., 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.