CREATINE KINASE (CK) - ANVISA Registration 81666810022

Access comprehensive regulatory information for CREATINE KINASE (CK) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81666810022 and manufactured by BIOANALÍTICA DIAGNÓSTICA LTDA. The registration is held by BIOANALÍTICA DIAGNÓSTICA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including GOLD ANALISA DIAGNOSTICA LTDA, KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO 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.