Bone Densitometry Device - ANVISA Registration 80071260163

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 80071260163 and manufactured by manufacturer not specified. The registration is held by GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA with validity until Jun 13, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including OSTEOSYS CO., LTD, 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.