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
 

 
 
9 records meeting your search criteria returned- Product Code: DRA Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER (CE) 03/13/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 02/09/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 06/21/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 03/30/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 06/24/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 03/25/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/06/2021
ABBOTT VASCULAR STEERABLE GUIDE CATHETER 07/15/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 11/12/2018
-
-