• 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 
 > 
 
17 records meeting your search criteria returned- Product Code: LJT Product Problem: Entrapment of Device Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (BASD) -3006260740 M.R.I. IMPLANTABLE PORT, HICKMAN SINGLE- 10/21/2022
ANGIODYNAMICS INC. SINGLE LUMEN STANDARD TITANIUM PORT 8 FR 04/22/2022
C.R. BARD, INC. (BASD) -3006260740 M.R.I. IMPLANTABLE PORT, HICKMAN SINGLE- 04/13/2022
BARD ACCESS SYSTEMS, INC. BARD POWER PORT 12/29/2021
BARD ACCESS SYSTEMS, INC. POWERPORT IMPLANTABLE PORT GROSHONG CATH 08/11/2021
B.BRAUN MEDICAL SAS CELSITE 07/09/2021
C.R. BARD, INC. (BASD) -3006260740 M.R.I. IMPLANTABLE PORT, HICKMAN SINGLE- 12/14/2020
BARD ACCESS SYSTEMS POWERPORT 07/20/2020
BARD ACCESS SYSTEMS, INC. POWERPORT ISP M.R.I. IMPLANTABLE PORT 07/14/2020
BARD ACCESS SYSTEMS X-PORT ISP IMPLANTABLE PORT, CHRONOFLEX 07/14/2020
-
-