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INTRACLUDE INTRA-AORTIC INCLUSION DEVICE. Anvisa Registration n ° 80219050151. Model ICF100.
Model / Serial
Manufacturer
Edwards Lifescience Comércio de Produtos Ltda; Edwards Lifesciences LLC
1 Event
Safety Alert for INTRACLUDE INTRA-AORTIC INCLUSION DEVICE. Anvisa Registration n ° 80219050151. Model ICF100.
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Manufacturer
Edwards Lifescience Comércio de Produtos Ltda; Edwards Lifesciences LLC
Manufacturer Parent Company (2017)
Edwards Lifesciences Corporation
Source
ANVSANVISA
Language
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