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

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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
103 records meeting your search criteria returned- Product Code: DTQ Patient Problem: Death Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH CARDIOHELP-I, US-VERSION 08/09/2019
MAQUET CARDIOPULMONARY GMBH CARDIOHELP-I, US-VERSION 08/09/2019
MAQUET CARDIOPULMONARY GMBH CARDIOHELP SYSTEM 04/01/2019
MAQUET CARDIOPULMONARY GMBH VARIO SINGLE, HL 20, 4-PUMPS 04/01/2019
MAQUET CARDIOPULMONARY GMBH CARDIOHELP-I 03/15/2019
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO ADVANCED PERFUSION SYSTEM 1 02/25/2019
MAQUET CARDIOPULMONARY AG CARDIOHELP SYSTEM 02/15/2019
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 02/07/2019
MAQUET CARDIOPULMONARY AG CARDIOHELP SYSTEM 12/26/2018
LIVANOVA DEUTSCHLAND S5 SYSTEM 07/26/2018
-
-