• 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 
 > 
 
25 records meeting your search criteria returned- Product Code: JAA Product Problem: Display or Visual Feedback Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS USA PHILLIPS BV PULSERA - C -ARM IMAGING SYS 08/12/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. COMBI DIAGNOST R90 02/28/2023
SIEMENS AG/SIEMENS HEALTHCARE GMBH SIEMENS ARTIS Q BIPLANE 02/06/2023
PHILIPS MEDICAL SYSTEMS DMC GMBH SYSTEM, X-RAY, FLUOROSCOPIC, IMAGE-INTEN 01/13/2023
PHILIPS MEDICAL SYSTEMS DMC GMBH COMBIDIAGNOST R90 09/29/2021
OEC MEDICAL SYSTEMS, INC. OEC 02/02/2021
SIEMENS HEALTHCARE GMBH ARTIS Q 01/29/2019
SIEMENS HEALTHCARE GMBH ARTIS Q BIPLANE 01/16/2019
GE OEC MEDICAL SYSTEMS (SLC) 9800 04/23/2015
GE OEC MEDICAL SYSTEMS (SLC) 9800 04/06/2015
-
-