Bipolar Forceps - ANVISA Registration 10355870324

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 10355870324 and manufactured by Katalyst Surgical, LLC. The registration is held by BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA with validity until Jan 14, 2029.

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.