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

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
 

 
 
8 records meeting your search criteria returned- Product Code: OJX Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
BIOTRONIK DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
ST. JUDE MEDICAL DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
ST. JUDE MEDICAL LEAD 08/09/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 07/19/2023
BIOTRONIK SE & CO. KG SENTUS PROMRI OTW QP L-75/49 01/09/2019
-
-