• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: DXE Product Problem: Mechanical Jam Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION SPIROFLEX ANGIOJET THROMBECTOMY SET 06/30/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 01/21/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT DISTA 10/06/2020
ARROW INTERNATIONAL INC. ARROW PERCUTANEOUS THROMBOLYTIC DEVICE S 11/26/2019
PENUMBRA, INC. INDIGO SYSTEM CAT3 ASPIRATION CATHETER 06/27/2018
PENUMBRA, INC. INDIGO SYSTEM CAT 8 ASPIRATION CATHETER 04/04/2018
PENUMBRA, INC. INDIGO SYSTEM CAT 6 ASPIRATION CATHETER 03/20/2018
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 12/12/2017
PENUMBRA, INC. INDIGO SYSTEM CAT 5 ASPIRATION CATHETER 12/11/2017
PENUMBRA, INC. INDIGO SYSTEM SEPARATOR 5 02/17/2017
-
-