• 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
 

 
 
 1 
 2 
 3 
 > 
 
22 records meeting your search criteria returned- Product Code: DRA Patient Problem: Tissue Damage Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 02/10/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/18/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 12/30/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 09/17/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 07/21/2020
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 06/03/2020
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 06/02/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/20/2020
ABBOTT VASCULAR STEERABLE GUIDE CATHETER 12/10/2019
ABBOTT VASCULAR STEERABLE GUIDE CATHETER 10/25/2019
-
-