Basic diagnostic radiology apparatus for manual, digital use - ANVISA Registration 80101380007

Access comprehensive regulatory information for Basic diagnostic radiology apparatus for manual, digital use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80101380007 and manufactured by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA. The registration is held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA with validity until Jun 13, 2026.

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 AGFA NV, GE MEDICAL SYSTEMS LLC, 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.