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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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2 records meeting your search criteria returned- Product Code: KFM Product Problem: Coagulation in Device or Device Ingredient Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH CENTRIFUGAL PUMP 03/15/2021
CARDIAC ASSIST INC. TANDEMHEART PUMP 04/18/2019
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