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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
135 records meeting your search criteria returned- Product Code: NBW Product Problem: Unsealed Device Packaging Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ASCENSIA DIABETES CARE US INC. CONTOUR NEXT 05/26/2016
ASCENSIA DIABETES CARE US INC. CONTOUR 05/11/2016
ASCENSIA DIABETES CARE US INC. CONTOUR 04/07/2016
ASCENSIA DIABETES CARE US INC. CONTOUR NEXT 02/25/2016
ASCENSIA DIABETES CARE US INC. CONTOUR 02/18/2016
BAYER HEALTHCARE LLC CONTOUR NEXT 01/04/2016
BAYER HEALTHCARE LLC CONTOUR NEXT 11/30/2015
BAYER HEALTHCARE LLC CONTOUR 11/11/2015
NIPRO DIAGNOSTICS, INC. BLOOD GLUCOSE SYSTEM 10/21/2015
LIFESCAN EUROPE, A DIVISION OF CILAG GMB OT VERIO TEST STRIPS 09/24/2015
-
-