Commercial name: Prodigy Lunar Bone Densitometer. ANVISA registry number: 80071260163. Class of risk: III. Affected model (s); and Lot (s) / Serial number (s) affected :. The following software versions: 15, 15 SP1, and 15 SP2 are affected by the products. - Bone Densitometer (Model: DPX - NT and Record: 80071260176). - Bone Densitometry System (Model: Lunar iDXA and Record: 80071260178). - Prodigy Lunar Bone Densitometer (Model: Prodigy, Prodigy Advance, Prodigy Primo and Prodigy Pro - Record: 80071260163).
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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