Hemostatic Forceps - ANVISA Registration 80475510248

Access comprehensive regulatory information for Hemostatic 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 80475510248 and manufactured by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME. The registration is held by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME with validity until Oct 05, 2030.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SCITECH PRODUTOS MEDICOS SA, EDWARDS LIFESCIENCES LLC, 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.