• 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
 

 
 
10 records meeting your search criteria returned- Product Code: LJT Product Problem: Reflux within 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 POWERPORT SLIM IMPLANTABLE PORT, CHRONOF 07/08/2022
C.R. BARD, INC. (BASD) -3006260740 POWERPORT ISP M.R.I. IMPLANTABLE PORT, G 02/24/2022
C.R. BARD, INC. (BASD) -3006260740 TITANIUM LOW-PROFILE IMPLANTABLE PORT, G 09/27/2021
C.R. BARD, INC. (BASD) -3006260740 POWERPORT SLIM IMPLANTABLE PORT, CHRONOF 09/06/2021
C.R. BARD, INC. (BASD) -3006260740 TITANIUM LOW-PROFILE IMPLANTABLE PORT, G 08/08/2021
C.R. BARD, INC. (BASD) -3006260740 POWERPORT ISP TI 8F CHRONWSH 07/29/2021
C.R. BARD, INC. (BASD) -3006260740 POWERPORT SLIM IMPLANTABLE PORT, CHRONOF 05/24/2021
BARD ACCESS SYSTEMS POWERPORT CLEARVUE SLIM IMPLANTABLE PORT 09/25/2020
BARD ACCESS SYSTEMS CHRONO TITANIUM PORT 07/17/2020
BARD ACCESS SYSTEMS POWERPORT ISP M.R.I. IMPLANTABLE PORT, G 07/17/2020
-
-