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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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54 records meeting your search criteria returned- Product Code: DQX Product Problem: Defective Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR HI TORQUE SUPRA CORE 35 12/23/2019
BOSTON SCIENTIFIC CORPORATION AMPLATZ SUPER STIFF 11/04/2019
PHILIPS / VOLCANO CORPORATION VERRATA PLUS PRESSURE GUIDE WIRE 09/30/2019
PHILIPS / VOLCANO CORPORATION VERRATA PLUS PRESSURE GUIDE WIRE 09/30/2019
AV-TEMECULA-CT 0.014 HI-TORQUE (HT) TURNTRAC GUIDE WIRE 06/14/2019
BOSTON SCIENTIFIC CORPORATION ACUITY MAILMAN 02/06/2019
AV-TEMECULA-CT HI-TORQUE SUPRA CORE 35 GUIDE WIRE WITH 01/30/2019
BOSTON SCIENTIFIC CORPORATION BACK-UP MEIER 11/12/2018
COOK INC ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUI 09/19/2018
COOK INC ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUI 09/18/2018
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