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Manufacturers
GE Healthcare do Brasil, Com. e Serv. para Equipamentos Médico-Hospitalares Ltda.; GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Manufacturer Parent Company (2017)
General Electric Company
Source
ANVSANVISA
1 Event
Safety Alert for 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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One device in the database
Commercial name: Bone Densitometry / Densitometer Osseo Lunar Dpx / Osseo Lunar Densitometer Dpx ...
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