• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
249 records meeting your search criteria returned- Product Code: LJT Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST PAUL PORT-A-CATH IMPLANTABLE ACCESS SYSTEM 08/02/2023
ST PAUL PORT-A-CATH IMPLANTABLE ACCESS SYSTEM 08/02/2023
C.R. BARD, INC. (BASD) -3006260740 POWER PORT MRI ISP, 8 FR. GROSHONG, INT 07/10/2023
C.R. BARD, INC. (BASD) -3006260740 POWERPORT CLEARVUE SLIM IMPLANTABLE PORT 06/29/2023
ANGIODYNAMICS VORTEX PORT 04/17/2023
ANGIODYNAMICS SMART PORT 03/30/2023
NAVILYST MEDICAL, INC. SMART PORT CT 03/21/2023
BARD ACCESS SYSTEMS, INC. PORT IMPLANTABLE - CHRONOFLEX CATHETER 6 02/14/2023
C.R. BARD, INC. (BASD) -3006260740 POWERPORT ISP M.R.I. IMPLANTABLE PORT, C 01/18/2023
ANGIODYNAMICS SMART PORT 12/29/2022
-
-