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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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8 records meeting your search criteria returned- Product Code: KFM Product Problem: Premature Discharge of Battery Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 10/05/2022
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 07/18/2022
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 03/14/2022
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 02/01/2022
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 12/13/2021
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 09/22/2021
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 07/14/2021
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 07/14/2021
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