Biopsy Forceps - ANVISA Registration 10334789012

Access comprehensive regulatory information for Biopsy Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10334789012 and manufactured by G-FLEX EUROPE SPRL (NIVELLES). The registration is held by G.F.E. DO BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including Jiuhong, CHANGZHOU HEALTH MICROPORT MEDICAL DEVICES CO.,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.