Biopsy Device - ANVISA Registration 82702709031

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82702709031 and manufactured by ENDO AMÉRICAS INDÚSTRIA E COMÉRCIO DE MATERIAL MÉDICO HOSPITALAR LTDA. The registration is held by ENDO AMÉRICAS INDÚSTRIA E COMÉRCIO DE MATERIAL MÉDICO HOSPITALAR 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 STERYLAB S.R.L., Zamar D.O.O., 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.