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
 

 
 
 1 
 2 
 > 
 
13 records meeting your search criteria returned- Product Code: FED Product Problem: Flaked Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 PROXIS¿ URETERAL ACCESS SHEATH 03/08/2023
C.R. BARD, INC. (COVINGTON) -1018233 PROXIS¿ URETERAL ACCESS SHEATH 02/07/2023
COOK INC FLEXOR URETERAL ACCESS SHEATH AND DILATO 01/20/2023
COOK INC FLEXOR URETERAL ACCESS SHEATH AND DILATO 10/04/2022
COOK INC FLEXOR URETERAL ACCESS SHEATH AND DILATO 06/29/2022
COOK INC FLEXOR PARALLEL URETERAL ACCESS SHEATH A 01/06/2022
COOK INC FLEXOR PARALLEL URETERAL ACCESS SHEATH A 12/16/2021
COOK INC FLEXOR URETERAL ACCESS SHEATH AND DILATO 11/24/2021
C.R. BARD, INC. (COVINGTON) -1018233 PROXIS URETERAL ACCESS SHEATH 01/26/2021
C.R. BARD, INC. (COVINGTON) -1018233 PROXIS¿ URETERAL ACCESS SHEATH 12/12/2019
-
-