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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
258 records meeting your search criteria returned- Product Code: DQO Product Problem: Break Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CORPORATION, ASHITAKA PROGREAT CATHETER 10/12/2020
BOSTON SCIENTIFIC CORPORATION RENEGADE STC 18 09/10/2020
MICROVENTION, INC. HEADWAY DUO MICROCATHETER 06/19/2020
ANGIODYNAMICS, INC. ANGIODYNAMICS ACCU-VU OMNI FLUSH CATHETE 06/01/2020
COOK INCORPORATED COOK 05/28/2020
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 05/15/2020
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 05/15/2020
CORDIS CORPORATION CORDIS 5F UF CATHETER 05/01/2020
ACCURATE MEDICAL THERAPEUTICS LTD. MICROCATHETER SEQURE 28 130 X1 04/22/2020
TERUMO CORPORATION GLIDECATH 04/02/2020
-
-