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
 

 
 
8 records meeting your search criteria returned- Product Code: NZU Product Problem: Leak/Splash Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C. R. BARD, INC. PUREWICK FEMALE EXTERNAL CATHETER 03/15/2021
BD/ C.R BARD PUREWICK FEMALE EXTERNAL CATHETER 01/20/2021
BD/ C.R BARD PUREWICK FEMALE EXTERNAL CATHETER 01/20/2021
C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL CATHETER 09/16/2020
C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL CATHETER 04/15/2020
C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL. 03/03/2020
C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL 10/31/2019
C.R. BARD, INC. (COVINGTON) -1018233 PUREWICK FEMALE EXTERNAL 10/10/2019
-
-