Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
10 records meeting your search criteria returned- Product Code: LJT Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
B.BRAUN MEDICAL SAS CELSITE 04/30/2024
B.BRAUN MEDICAL SAS CELSITE 04/30/2024
B.BRAUN MEDICAL SAS CESLITE 12/08/2023
C.R. BARD, INC. (BASD) -3006260740 UNKNOWN PORT 10/20/2020
C.R. BARD, INC. (BASD) -3006260740 UNKNOWN PORT 10/09/2020
BARD ACCESS SYSTEMS POWERPORT ISP M.R.I. IMPLANTABLE PORT, C 10/01/2020
BARD ACCESS SYSTEMS POWERPORT ISP M.R.I. IMPLANTABLE PORT, C 09/29/2020
BARD ACCESS SYSTEMS POWERPORT SLIM IMPLANTABLE PORT, CHRONOF 09/04/2020
B.BRAUN MEDICAL SAS CELSITE 07/11/2019
PFM MEDICAL CPP SA XCELA POWER INJECTABLE PORT 02/06/2019
-
-