• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 
 
70 records meeting your search criteria returned- Product Code: DXE Product Problem: Device Handling Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 09/30/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 09/14/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 8 08/30/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 08/11/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 07/21/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 07/01/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION TUBING 06/23/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 06/14/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 6 06/10/2016
PENUMBRA, INC. INDIGO SYSTEM ASPIRATION CATHETER 8 06/02/2016
-
-