• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: DQX Product Problem: Connection Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO RADIFOCUS 08/12/2023
PHILIPS IMAGE GUIDED THERAPY CORPORATION OMNIWIRE 01/12/2023
PHILIPS IMAGE GUIDED THERAPY CORPORATION OMNIWIRE PRESSURE GUIDE WIRE, STRAIGHT T 10/13/2022
PHILIPS IMAGE GUIDED THERAPY CORPORATION OMNIWIRE PRESSURE GUIDE WIRE, STRAIGHT T 04/26/2022
ARROW INTERNATIONAL, INC. (SUBSIDIARY OF ARROW RADIAL ARTERY CATHETERIZATION SE 12/29/2021
BOSTON SCIENTIFIC CORPORATION COMET II 03/10/2021
ST. JUDE MEDICAL PRESSURE WIRE CERTUS G8 02/01/2021
ARROW INTERNATIONAL INC. ARROW RA CATH KIT: 20 GA X 1-1/2" 02/26/2020
VOLCARICA S.R.L. VERRATA PLUS PRESSURE GUIDE WIRE 07/16/2019
BOSTON SCIENTIFIC CORPORATION ACUITY WHISPER VIEW 02/08/2019
-
-