Craniotomes - ANVISA Registration 81770370013

Access comprehensive regulatory information for Craniotomes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81770370013 and manufactured by CODMAN & SHURTLEFF INC. The registration is held by INTEGRA LIFESCIENCES BRAZIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including G C DE ALMEIDA E CIA LTDA - ME, NOUVAG AG, and 3 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.