External Fixators - ANVISA Registration 82117660024

Access comprehensive regulatory information for External Fixators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82117660024 and manufactured by AIKE (SHANGHAI) MEDICAL INSTRUMENT CO., LTD. The registration is held by BFIX INTERNACIONAL COMERCIAL IMPORTADORA DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.