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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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118 records meeting your search criteria returned- Product Code: QAN Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
COVIDIEN ABRE VENOUS SELF-EXPANDING STENT SYSTEM 03/20/2024
COOK IRELAND LTD ZILVER VENA VENOUS SELF-EXPANDING STENT 03/20/2024
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG VENOVO VENOUS STENT 03/18/2024
COOK IRELAND LTD ZILVER VENA VENOUS SELF-EXPANDING STENT 03/15/2024
COVIDIEN ABRE VENOUS SELF-EXPANDING STENT SYSTEM 02/29/2024
COVIDIEN ABRE VENOUS SELF-EXPANDING STENT SYSTEM 12/22/2023
COVIDIEN ABRE VENOUS SELF-EXPANDING STENT SYSTEM 11/24/2023
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG VENOVO VENOUS STENT 10/16/2023
BOSTON SCIENTIFIC CORPORATION VENOUS WALLSTENT 10/12/2023
COOK IRELAND LTD ZILVER VENA VENOUS SELF EXPANDING STENT 10/10/2023
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