• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
52 records meeting your search criteria returned- Product Code: GEA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. 0 ENDOLOOP LIG W/PDS II 01/12/2023
ETHICON INC. 0 ENDOLOOP LIG W/PDS II 01/12/2023
ETHICON INC. ENDO SUTURE UNKNOWN PRODUCT 11/07/2022
ETHICON INC. ENDOLOOP LIGATURE UNKNOWN PRODUCT 10/26/2022
ETHICON INC. 0 ENDOLOOP LIG W/PDS II 10/11/2022
ETHICON INC. 0 ENDOLOOP LIG W/PDS II 08/12/2022
ETHICON INC. ENDOLOOP LIGATURE UNKNOWN PRODUCT 07/06/2022
SYNTHES GMBH ACCESS KIT 4.7 06/09/2022
ETHICON INC. ENDOLOOP LIGATURE UNKNOWN PRODUCT 12/15/2021
ETHICON INC. ENDOLOOP LIG PDS II VIO SUT 11/08/2021
-
-