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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
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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8 records meeting your search criteria returned- Product Code: KFM Product Problem: No Apparent Adverse Event Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 11/28/2022
THORATEC SWITZERLAND GMBH PEDIMAG BLOOD PUMP 06/14/2022
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 05/31/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 12/15/2021
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 12/02/2021
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 07/13/2021
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 03/30/2021
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 11/29/2018
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