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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: DQX Product Problem: Unintended Movement Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC AMPLATZ SUPER STIFF GUIDEWIRE 08/12/2023
BOSTON SCIENTIFIC AMPLATZ SUPER STIFF GUIDEWIRE 08/12/2023
GADELUIS MEDICAL WIRE, GUIDE, CATHETER 08/12/2023
ST JUDE MEDICAL WIRE, GUIDE, CATHETER 08/12/2023
COOK INC AMPLATZ EXTRA-STIFF SUPPORT WIRE GUIDE 03/05/2019
CORDI CORP CORDIS ATW 10/14/2014
LAKE REGION MEDICAL PREFORM GUIDEWIRE 02/05/2014
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