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 Patient Problem: No Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ANGIODYNAMICS BIOFLO PORT 01/05/2021
ST PAUL DELTEC 09/03/2020
B.BRAUN MEDICAL SAS CELSITE 06/15/2020
MEDICAL COMPONENTS, INC. 8F DIGNITY CT PORT 02/04/2020
MEDICAL COMPONENTS, INC. 8F DIGNITY CT PORT 09/04/2019
C. R. BARD, INC. BARD PORT IMPLANTED PORT WITH GROSHONG C 08/08/2019
SMITHS MEDICAL ASD, INC. DELTEC PORT-A-CATH II POWER P.A.C 06/14/2019
PFM MEDICAL CPP SA XCELA 02/05/2019
PFM MEDICAL CPP SA XCELA 02/05/2019
Unknown Manufacturer UNKNOWN 01/23/2019
-
-