• 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 
 7 
 8 
 9 
 10 
 > 
 
237 records meeting your search criteria returned- Product Code: DQO Patient Problem: Foreign Body In Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CLINICAL SUPPLY CO., LTD. ZIZAI 04/19/2023
MERIT MEDICAL SYSTEMS, INC. IMPRESS® 04/12/2023
ANGIODYNAMICS SOFT-VU SIZING ANGIOGRAPHIC CATHETER 03/30/2023
MERIT MEDICAL SYSTEMS INC. IMPRESS® BRAIDED CATHETER 03/24/2023
TERUMO MEDICAL CORPORATION PROGREAT CATHETER 03/23/2023
COOK, INC. ADVANTAGE CATHETER TORCON NB 03/07/2023
MERIT MEDICAL SYSTEMS IMPRESS® 03/06/2023
MERIT MEDICAL SYSTEMS, INC. PERFORMA® 03/06/2023
COOK INC ROYAL FLUSH PLUS FLUSH CATHETER 02/28/2023
MERIT MEDICAL SYSTEMS, INC. IMPRESS® 02/21/2023
-
-