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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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7 records meeting your search criteria returned- Product Code: DTM Patient Problem: No Information Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
TERUMO CORPORATION, ASHITAKA ARTERIAL FILTER 06/28/2019
TERUMO CORPORATION, ASHITAKA UNK CAPIOX ARTERIAL FILTER 04/08/2019
MAQUET CARDIOPULMONARY AG VENOUS HARDSHELL CARDIOTOMY RESERVOIR 05/23/2018
BERND RAKOW RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS 01/08/2018
MAQUET CARDIOPULMONARY AG RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS 09/11/2017
MAQUET CARDIOPULMONARY AG VENOUS HARDSHELL CARDIOTOMY RESERVOIR 08/28/2017
SORIN GROUP/LIVANOVA LIVANOVA 04/21/2017
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