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

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 
 3 
 4 
 5 
 6 
 > 
 
57 records meeting your search criteria returned- Product Code: DTZ Product Problem: Disconnection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY AG QUADROX-ID ADULT DIFFUSION MEMBRANE OXY. 07/28/2015
MAQUET CARDIOPULMONARY AG QUADROX-ID ADULT DIFFUSION MEMBRANE OXY. 07/28/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP. STERILE FX25RW OX W / RES 05/07/2015
TERUMO CARDIOVASCULAR SYSTEMS CORP. STERILE FX25RW OX W/ RES 05/07/2015
TERUMO CORP, ASHITAKA FX OXY W/HR AND ART FILTER 06/27/2014
TERUMO CORPORATION, ASHITAKA FX OXY W/HR & ART FILTER 06/23/2014
TERUMO CORP FX OXY W/HR & ART FILTER 05/30/2014
TERUMO CORP, ASHITAKA FX OXY W/HR & ART FILTER 05/30/2014
TERUMO CORPORATION FX OXY W/HR & ART FILTER 04/09/2014
TERUMO CORPORATION FX OXY W/RA & ART FILTER 04/09/2014
-
-