Devices - ANVISA Registration 80213730012

Access comprehensive regulatory information for Devices in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80213730012 and manufactured by Clinical Resolution Laboratory, Inc.. The registration is held by FABINJECT INDÚSTRIA E COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO LTDA - EPP 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 APPLIED MEDICAL TECHNOLOGY, INC, ATOS MEDICAL AB, 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.