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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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8 records meeting your search criteria returned- Product Code: FAD Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 URETERAL STENTS 02/26/2020
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY OPTIMA® MULTILENGTH URETERAL 10/29/2019
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY® URETERAL STENT 09/12/2019
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY® URETERAL STENT WITH HYDROGL 08/09/2019
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY OPTIMA® URETERAL STENT WITH 05/28/2019
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY OPTIMA® URETERAL STENT WITH 03/16/2018
COOK IRELAND LTD RESONANCE STENT SET 03/10/2016
COOK IRELAND LTD RESONANCE STENT SET 03/10/2016
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