• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
233 records meeting your search criteria returned- Product Code: DSQ Patient Problem: Septic Shock Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - PU 10/25/2021
THORATEC CORPORATION HEARTMATE 3 LVAS IMPLANT KIT 10/21/2021
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - PU 10/21/2021
THORATEC CORPORATION HEARTMATE 3 LVAS IMPLANT KIT 10/19/2021
THORATEC CORPORATION HEARTMATE 3 LVAS IMPLANT KIT 10/06/2021
THORATEC CORPORATION HEARTMATE 3 LVAS IMPLANT KIT 09/29/2021
THORATEC CORPORATION HEARTMATE 3 LVAS IMPLANT KIT 09/27/2021
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - PU 09/27/2021
THORATEC CORPORATION HEARTMATE II LVAS IMPLANT KIT (WITH SEAL 09/25/2021
THORATEC CORPORATION THORATEC HEARTMATE 3 LVAD 09/21/2021
-
-