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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 
 
60 records meeting your search criteria returned- Product Code: FOS Product Problem: Break Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN 5.0FR URETHANE UMB CATH 08/13/2019
UTAH MEDICAL PRODUCTS, INC. UMBILI-CATH 07/19/2019
UTAH MEDICAL PRODUCTS, INC. UMBILI-CATH 06/07/2019
VYGON UMBILICAL CATHETER 05/28/2019
UTAH MEDICAL PRODUCTS, INC. UMBILI-CATH 05/10/2019
COVIDIEN 5FR DUAL-LUMEN UVC CATH 01/24/2019
COVIDIEN 5.0FR URETHANE UMB CATH 01/16/2019
COVIDIEN 3.5FR URETHANE UMB CATH 01/16/2019
COVIDIEN 3.5FR URETHANE UMB CATH 01/09/2019
COVIDIEN ARGYLE 01/08/2019
-
-