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Abiomed is recalling the labeling for Impella RP Flex with Smart Assist System Catheter because the catheters’ Instructions for Use (IFU) do not appropriately address precautions for healthcare providers to take when treating patients whose anticoagulation clotting time is below the recommended value 

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,Abiomed Clinical Support Center ,Drug Administration ,Abiomed ,Adverse Event Reporting Program ,Smart Assist System Catheter ,Recall Database ,Smartassist Catheters ,Important Medical Device Advisory ,White Blood Cell ,Deep Vein Thrombosis ,Extracorporeal Membrane Oxygenation ,Clinical Support Center ,

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