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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 HOLLOW FIBER OXYGENATOR/ARTERIAL 10/05/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 10/05/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO HOLLOW FIBER OXY WITH 3000 ML 09/10/2021
TERUMO CORPORATION, ASHITAKA CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL 09/03/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 06/25/2021
TERUMO CORPORATION, ASHITAKA CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL 06/24/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 4L RES 06/23/2021
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 06/01/2021
MAQUET CARDIOPULMONARY GMBH HLS SET ADVANCED 06/01/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 05/26/2021
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