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: FAD Product Problem: Device Markings/Labelling Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COLOPLAST A/S IMAJIN SILICONE HYDRO-COATED DOUBLE LOOP 06/08/2023
COLOPLAST A/S BIOSOFT DUO DOUBLE LOOP STENT 05/19/2023
COLOPLAST A/S VORTEK DOUBLE LOOP URETERAL STENT 03/29/2023
COLOPLAST A/S VORTEK DOUBLE LOOP URETERAL STENT 03/27/2023
COLOPLAST A/S VORTEK DOUBLE LOOP URETERAL STENT 03/27/2023
COLOPLAST A/S VORTEK DOUBLE LOOP URETERAL STENT 03/27/2023
COLOPLAST A/S IMAJIN DOUBLE LOOP URETERAL STENT 02/03/2022
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY OPTIMA® MULTILENGTH URETERAL 12/12/2019
C.R. BARD, INC. (COVINGTON) -1018233 BARD® INLAY OPTIMA® MULTILENGTH URETERAL 08/15/2019
-
-