Bone Densitometry Device - ANVISA Registration 80047300540

Access comprehensive regulatory information for Bone Densitometry Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80047300540 and manufactured by OSTEOSYS CO., LTD. The registration is held by MEDSTAR IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until Mar 16, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC, HOLOGIC, INC, and 4 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.