• 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
 

 
 
9 records meeting your search criteria returned- Product Code: IZI Product Problem: Mechanical Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEEGO 10/28/2016
PHILIPS MEDICAL SYSTEMS PHILIPS MEDICAL SYSTEMS 10/13/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE FLOOR 07/08/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE FLOOR 07/08/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE BIPLANE 06/01/2016
SIEMENS HEALTHCARE, BUSINESS AREA ADVANC ARTIS ZEE CEILING 02/12/2016
PHILIPS HEALTHCARE ALLURA XPER FD20 07/21/2014
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10 07/01/2014
PHILIPS HEALTHCARE ALLURA ZPER FD20 06/02/2014
-
-