Devices

Commercial name: Bone Densitometry / Densitometer Osseo Lunar Dpx / Osseo Lunar Densitometer Dpx / Bone Densitometer Prodigy. Technical Name: Bone Desensiometry Apparatus. ANVISA registration number: 80071260174; 80071260176; 80035360019; 80071260163 ;. Risk class: III. Affected Model: DPX Bravo, DPX-Duo (80071260174) / DPX-NT (80071260176) / DPX-MD + (80035360019) / Prodigy, Prodigy Advance (80071260163). Lots of numbers affected: PA + 130268; LNR41569; LNR74315; LNR150180; LNR73479

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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Manufacturer

GE Healthcare do Brasil, Com. e Serv. para Equipamentos Médico-Hospitalares Ltda.; GE Medical Sys...