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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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110 records meeting your search criteria returned- Product Code: DTZ Product Problem: Coagulation in Device or Device Ingredient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 05/29/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 05/07/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 01/19/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 01/09/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 08/11/2017
TERUMO CORPORATION, ASHITAKA CAPIOX RX OXYGENATOR 06/28/2017
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 HOLLOW FIBER OXYGENATOR 11/09/2016
TERUMO CORPORATION, ASHITAKA CAPIOX FX 15 HOLLOW FIBER OXYGENATOR AF 08/12/2016
MAQUET CARDIOPULMONARY AG QUADROX-ID PEDIATRIC DIFFUSION MEMBRANE 07/14/2016
MEDTRONIC PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 06/15/2016
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