Endoscopic Forceps - ANVISA Registration 80005430048

Access comprehensive regulatory information for Endoscopic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80005430048 and manufactured by STRYKER TRAUMA GMBH (SCHONKIRCHEN). The registration is held by STRYKER DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 10 related devices, regulatory compliance details, 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.