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
 

 
 
5 records meeting your search criteria returned- Product Code: DRC Patient Problem: Insufficient Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL TROCAR 08/12/2023
MEDTRONIC BROCKENBROUGH CURVED NEEDLE 08/12/2023
ST. JUDE BRK-TRANSSEPTAL NEEDLE 08/12/2023
UNKNOWN BROCKENBROUGH 07/26/2023
COOK INC ONE-PART PERCUTANEOUS ENTRY NEEDLE 02/07/2023
-
-