• 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 
 > 
 
227 records meeting your search criteria returned- Product Code: DXY Product Problem: Premature Elective Replacement Indicator Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SORIN CRM SYMPHONY 06/21/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY REPLY 03/02/2017
BIOTRONIK SE & CO. KG KALOS DR 05/13/2016
ST. JUDE MEDICAL, INC., CRMD ACCENT DR 03/02/2015
ST. JUDE MEDICAL, INC., CRMD ASSURITY SR 03/02/2015
ST. JUDE MEDICAL, INC., CRMD SUSTAIN XL DR 03/02/2015
ST. JUDE MEDICAL, INC., CRMD EMPRISE SR+ 02/25/2015
BIOTRONIK SE & CO. KG CYLOS DR 02/23/2015
ST. JUDE MEDICAL, INC., CRMD SUSTAIN XL DR 01/07/2015
ST. JUDE MEDICAL, INC., CRMD ACCENT MRI DR 01/06/2015
-
-