Instrumentation for Spinal Fixation - ANVISA Registration 81022030010

Access comprehensive regulatory information for Instrumentation for Spinal Fixation in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81022030010 and manufactured by SINTEA PLUSTEK S.R.L.. The registration is held by SOLLIEVO MEDICINA ESPECIALIZADA 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 EUROSURGICAL SPINENETWORK, SOLCO BIOMEDICAL 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.