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 
 > 
 
12 records meeting your search criteria returned- Product Code: DTQ Product Problem: Improper Device Output Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO ADVANCED PERFUSION SYSTEM 1 09/22/2017
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO ADVANCED PERFUSION SYSTEM 1 08/16/2017
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO ADVANCED PERFUSION SYSTEM 1 08/16/2017
LIVANOVA DEUTSCHLAND S5 CARDIOPLEGIA SENSOR MODULE 04/05/2017
SORIN GROUP DEUTSCHLAND SORIN S5 SYSTEM 09/28/2016
SORIN GROUP DEUTSCHLAND SORIN S5 SYSTEM 09/28/2016
SORIN GROUP DEUTSCHLAND SORIN S5 SYSTEM 06/03/2016
MAQUET CARDIOPULMONARY AG ROTAFLOW CENTRIFUGAL PUMP SYSTEM 12/23/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP. TERUMO ADVANCED PERFUSION SYSTEM 1 12/21/2015
MAQUET CARDIOPULMONARY AG MCP00952291#ROTAFLOW DRIVE UNIT, BLUE 05/18/2015
-
-