• 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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
308 records meeting your search criteria returned- Product Code: FOZ Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECTON DICKINSON MEDICAL (SINGAPORE) BD PEGASUS¿ SAFETY CLOSED IV CATHETER SY 05/24/2018
BECTON DICKINSON INDUSTRIAS CIRURGICAS, BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHET 05/22/2018
BECTON, DICKINSON AND COMPANY BD NEXIVA, BD Q-SYTE 05/22/2018
BECTON DICKINSON INFUSION THERAPY SYSTEM BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHET 05/15/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD SAF-T-INTIMA IV CATHETER SAFETY SYSTE 05/15/2018
BECTON DICKINSON INFUSION THERAPY SYSTEM BD INSYTE AUTOGUARD BC ANGIOCATH 05/15/2018
TERUMO CORPORATION - KOFU TERUMO SURFLASH I.V . CATHETER 05/15/2018
BECTON DICKINSON INFUSION THERAPY SYSTEM BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHET 05/11/2018
BD (SUZHOU) BD PEGASUS¿ SAFETY CLOSED IV CATHETER SY 05/07/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD SAF-T-INTIMA¿ IV CATHETER SAFETY SYST 05/07/2018
-
-