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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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160 records meeting your search criteria returned- Product Code: KFM Product Problem: Mechanical Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH PEDIMAG BLOOD PUMP 07/21/2023
THORATEC SWITZERLAND GMBH PEDIMAG BLOOD PUMP 07/10/2023
PERFUSION SYSTEMS AFFINITY AP40 CENTRIFUGAL PUMP 07/03/2023
THORATEC SWITZERLAND GMBH CMAG BLOOD PUMP 06/23/2023
PERFUSION SYSTEMS AFFINITY CP PUMP 06/22/2023
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 06/01/2023
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP, CAN 05/24/2023
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 04/03/2023
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 04/03/2023
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 03/23/2023
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