Acerca de la base de datos
¿Cómo usar la IMDD?
Descargar la data
Preguntas frecuentes
Créditos
Manufacturers
GE Healthcare do Brasil, Com. e Serv. para Equipamentos Médico-Hospitalares Ltda.; GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Empresa matriz del fabricante (2017)
General Electric Company
Source
ANVSANVISA
1 Event
Alerta De Seguridad para 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
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Un dispositivo en la base de datos
Commercial name: Bone Densitometry / Densitometer Osseo Lunar Dpx / Osseo Lunar Densitometer Dpx ...
Modelo / Serial
Language
English
Français
Español
한국어