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 
 3 
 4 
 > 
 
37 records meeting your search criteria returned- Product Code: GDW Product Problem: Failure to Calibrate Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 10/16/2017
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 10/12/2017
COVIDIEN LP LLC NORTH HAVEN SIGNIA 09/28/2017
COVIDIEN LP LLC NORTH HAVEN SIGNIA 09/27/2017
COVIDIEN NORTH HAVEN - MFG IDRIVE ULTRA 08/08/2017
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 08/08/2017
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 08/08/2017
COVIDIEN, FORMERLY US SURGICAL A DIVISON ENDO GIA ADAPTER STANDARD 03/15/2017
COVIDIEN, FORMERLY US SURGICAL A DIVISON IDRIVE ULTRA POWERED HANDLE 1 01/13/2017
COVIDIEN, FORMERLY US SURGICAL A DIVISON ENDO GIA ADAPTER STANDARD 01/11/2017
-
-