• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
129 records meeting your search criteria returned- Product Code: MDI Patient Problem: Unspecified Infection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES BRANDYWINE TI DISTRACTION LOCK 05/31/2017
SYNTHES BRANDYWINE TI RIB SLEEVE-SIZE 10 220MM RADIUS 05/31/2017
SYNTHES BRANDYWINE 90 DEG TI S-HOOK/LEFT 05/31/2017
SYNTHES BRANDYWINE TI SUPERIOR CRADLE 220MM RADIUS 05/31/2017
SYNTHES BRANDYWINE TI DISTRACTION LOCK 05/31/2017
SYNTHES BRANDYWINE 90 DEG TI S-HOOK/RIGHT 05/31/2017
SYNTHES BRANDYWINE TI SUPERIOR CRADLE 220MM RADIUS 05/31/2017
SYNTHES BRANDYWINE TI DISTRACTION LOCK 05/31/2017
SYNTHES BRANDYWINE TI LUMBAR EXTENSION SIZE 11/220MM RADIUS 05/31/2017
SYNTHES BRANDYWINE TI CRADLE LOCK 05/31/2017
-
-