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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 FX25 HOLLOW FIBER OXYGENATOR AF 10/01/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP STERILE FX25RE OX W/ RES 09/15/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP STERILE FX25RE OX W/ RES 09/15/2015
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 HOLLOW FIBER OXYGENATOR AF 08/18/2015
MAQUET CARDIOPULMONARY AG QUADROX-ID ADULT DIFFUSION MEMBRANE OXY. 07/28/2015
MAQUET CARDIOPULMONARY AG QUADROX-I ADULT WITH VENOUS HARDSHELL CA 07/28/2015
MAQUET CARDIOPULMONARY AG QUADROX-ID ADULT DIFFUSION MEMBRANE OXY. 07/28/2015
TERUMO CORPORATION, ASHITAKA CAPIOX FX15 HOLLOW FIBER OXYGENATOR 07/22/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP. STERILE FX25RW OX W/RES 07/20/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP. STERILE FX15RE OX W/ 4L RES 07/09/2015
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