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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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50 records meeting your search criteria returned- Product Code: GDW Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
COVIDIEN EEA 06/30/2023
COVIDIEN LP GIA 01/25/2023
COVIDIEN TRI-STAPLE 2.0 11/21/2022
US SURGICAL PUERTO RICO PREMIUM PLUS CEEA 09/23/2022
COVIDIEN LP LLC NORTH HAVEN TRI-STAPLE 2.0 10/19/2021
ETHICON ENDO-SURGERY, LLC ETHICON ENDOSCOPIC MULTIPLE CLIP APPLIER 09/28/2021
ETHICON ENDO-SURGERY, LLC. BLUE RELOAD FOR ECHELON 60 10/21/2020
ETHICON ENDO-SURGERY, LLC. GST GREEN RELOAD, 60MM, 6 ROW 09/09/2020
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 340MM SHAFT 06/04/2020
ETHICON ENDO-SURGERY, LLC. WHITE RELOAD FOR ECHELON 45 05/07/2020
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