• 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: JAA Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE GMBH UROSKOP OMINA 12/06/2021
SIEMENS HEALTHCARE GMBH AXIOM ICONOS R200 11/30/2021
CANON MEDICAL SYSTEMS CORPORATION CANON 07/16/2020
SIEMENS HEALTHCARE GMBH UROSKOP OMNIA MAX 04/19/2019
SIEMENS HEALTHCARE GMBH LUMINOS AGILE MAX 04/17/2019
GE OEC MEDICAL SYSTEMS 9900 12/31/2014
SIEMENS HEALTHCARE AXIOM ICONOS R200 02/12/2014
SIEMENS HEALTHCARE AXIOM SIRESKOP SD 01/13/2014
-
-