• 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
 

 
 
8 records meeting your search criteria returned- Product Code: IZI Patient Problem: Radiation Overdose Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS HEALTHCARE ALLURA XPER FD10 09/14/2020
PHILIPS HEALTHCARE ALLURA XPER FD10/10 05/25/2020
SIEMENS HEALTHCARE GMBH ARTIS Q BIPLANE 04/19/2019
PHILIPS HEALTHCARE ALLURA XPER FD10 01/20/2017
PHILIPS HEALTHCARE ALLURA XPER FD10 12/21/2016
GE MEDICAL SYSTEMS SCS INNOVA IGS630 03/17/2016
GE MEDICAL SYSTEMS SCS INNOVA IGS 540 12/26/2014
SIEMENS AG SIEMENS ARTIS Q. ZEN 02/27/2014
-
-