• 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 
 
 
31 records meeting your search criteria returned- Product Code: IYE Product Problem: Unintended System Motion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
ELEKTA LTD ELEKTA SYNERGY 06/13/2017
SIEMENS HEALTHCARE GMBH ACCELERATOR, LINEAR, MEDICAL 11/02/2016
SIEMENS HEALTHCARE GMBH ONCOR IMPRESSION PLUS 11/05/2015
VARIAN LINEAR ACCELERATOR 05/01/2015
-
-