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

Manufacturer and User Facility Device Experience (MAUDE)

  • 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
344 records meeting your search criteria returned- Product Code: GEI Product Problem: No Apparent Adverse Event Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN MFG DC BOULDER FORCEFX 06/10/2023
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 LARGE JAW TISSUE SEALER 06/06/2023
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 CURVED 37CM SHAFT 04/20/2023
COVIDIEN MFG DC BOULDER FORCETRIAD 04/17/2023
COVIDIEN MFG DC BOULDER FORCE FX 03/17/2023
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 03/15/2023
APPLIED MEDICAL RESOURCES EB215, VOYANT MARYLAND FUSION 37CM, 6/BX 02/28/2023
KARL STORZ SE & CO. KG SUCTION AND COAG.CANNULA,L. 36 CM 02/28/2023
KARL STORZ SE & CO. KG SUCTION AND COAG.CANNULA,L. 36 CM 02/28/2023
CONMED UTICA AVANOS, DISPERSIVE ELECTRODE, THERMOGARD 02/24/2023
-
-