Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
10 records meeting your search criteria returned- Product Code: DXE Patient Problem: Thrombosis/Thrombus Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC, INC EXPORT AP ASPIRATION CATHETER 08/04/2023
MERIT MEDICAL SYSTEMS, INC. ASAP® 02/02/2023
MEDTRONIC, INC EXPORT AP ASPIRATION CATHETER 01/11/2023
MEDTRONIC, INC EXPORT UNKNOWN 06/09/2022
MEDTRONIC, INC EXPORT AP ASPIRATION CATHETER 03/03/2022
MEDTRONIC, INC EXPORT AP ASPIRATION CATHETER 02/22/2022
MEDTRONIC, INC ADVANCE 12/14/2021
TERUMO CLINICAL SUPPLY CO., LTD. ELIMINATE PLUS 10/02/2021
MEDTRONIC, INC EXPORT AP ASPIRATION CATHETER 09/07/2021
TERUMO CLINICAL SUPPLY CO., LTD. ELIMINATE 08/27/2021
-
-