• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: DRX Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONMED UTICA INVISITRACE ADULT MONITORING ELECTRODE ( 05/07/2022
CONMED UTICA INVISITRACE ADULT MONITORING ELECTRODE ( 03/15/2022
D. O. WEAVER AND COMPANY NUPREP 06/08/2020
CONMED CORPORATION CLEARTRACE; 5; TP, ADGEL 08/23/2019
CONMED CORPORATION CLEARTRACE 10 ELECTRODE 05/05/2017
CONMED CORPORATION CLEARTRACE 10 ELECTRODES 04/25/2017
NEOTECH NEOTECH 01/26/2017
NEOTECH NEOTECH 12/06/2016
NEOTECH NEOTECH 11/10/2016
NEOTECH NEOTECH 11/10/2016
-
-