• 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 
 > 
 
26 records meeting your search criteria returned- Product Code: MOF Product Problem: Break Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SCIENTIA VASCULAR ARISTOTLE 04/10/2024
SCIENTIA VASCULAR ARISTOTLE 04/04/2024
BALT EXTRUSION HYBRID GUIDEWIRE 03/20/2024
BALT USA HYBRID GUIDEWIRE 03/12/2024
BALT USA HYBRID GUIDEWIRE 02/16/2024
BALT USA HYBRID GUIDEWIRE 02/16/2024
BALT EXTRUSION HYBRID GUIDEWIRE 01/25/2024
SCIENTIA VASCULAR ARISTOTLE 14 11/15/2023
BALT USA HYBRID GUIDEWIRE 11/03/2023
BALT EXTRUSION HYRBID GUIDEWIRE 10/05/2023
-
-