Bipolar Forceps - ANVISA Registration 80071910120

Access comprehensive regulatory information for Bipolar Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80071910120 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Sep 16, 2034.

This page provides complete technical specifications for this device, 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.