Cannula Fixator - ANVISA Registration 80622210010

Access comprehensive regulatory information for Cannula Fixator in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80622210010 and manufactured by BIOFLORENCE IMPLEMENTOS ORTOPEDICOS LTDA. The registration is held by BIOFLORENCE IMPLEMENTOS ORTOPEDICOS 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 HOLLISTER INCORPORATED (ILLINOIS), MAGNA INDUSTRIA DE MATERIAIS HOSPITALARES LTDA, 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.