• 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
 

 
 
 1 
 2 
 > 
 
15 records meeting your search criteria returned- Product Code: DTM Report Date From: 1/1/2017 Report Date To: 12/31/2017

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY AG QUART ARTERIAL FILTER WITH SOFTLINE COAT 12/21/2017
MAQUET CARDIOPULMONARY AG RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS 12/04/2017
TERUMO CORPORATION, ASHITAKA CAPIOX ARTERIAL FILTER 10/19/2017
TERUMO CORPORATION, ASHITAKA CAPIOX ARTERIAL FILTER 10/19/2017
MAQUET CARDIOPULMONARY AG RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS 09/11/2017
MAQUET CARDIOPULMONARY AG VENOUS HARDSHELL CARDIOTOMY RESERVOIR 08/28/2017
MAQUET CARDIOPULMONARY AG VENOUS HARDSHELL CARDIOTOMY RESERVOIR 07/25/2017
MAQUET CARDIOPULMONARY AG RESERVOIR,BLOOD,CARDIOPULMONARY BYPASS 07/11/2017
MAQUET CARDIOPULMONARY AG BE-HQV 33800#COMPLETE PACK 04/26/2017
SORIN GROUP/LIVANOVA LIVANOVA 04/21/2017
-
-