Endoscopic Forceps - ANVISA Registration 81037940138

Access comprehensive regulatory information for Endoscopic 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 81037940138 and manufactured by RICHARD WOLF GMBH. The registration is held by RICHARD WOLF BRASIL EQUIPAMENTOS MEDICINAIS LTDA with validity until Apr 19, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RICHARD WOLF GMBH, 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.