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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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83 records meeting your search criteria returned- Product Code: FGE Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ZIMMON BILIARY STENT 01/18/2024
COOK IRELAND LTD EVOLUTION® BILIARY CONTROLLED-RELEASE ST 07/11/2023
COOK IRELAND LTD ZILVER 635 BILIARY SELF EXPANDING METAL 06/28/2023
COOK IRELAND LTD ZIMMON BILIARY STENT 06/21/2023
COOK IRELAND LTD ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUN 06/02/2023
COOK IRELAND LTD EVOLUTION® BILIARY CONTROLLED-RELEASE ST 05/24/2023
COOK IRELAND LTD OASIS ONE ACTION STENT INTRODUCTION SYST 08/25/2022
COOK INC ULTRATHANE MAC-LOC LOCKING LOOP BILIARY 07/25/2022
COOK IRELAND LTD OASIS ONE ACTION STENT INTRODUCTION SYST 06/30/2022
COOK IRELAND LTD OASIS ONE ACTION STENT INTRODUCTION SYST 06/01/2022
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