• 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 
 > 
 
53 records meeting your search criteria returned- Product Code: DQY Product Problem: Partial Blockage Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARROW INTERNATIONAL INC. ARROW ARTERIAL CATH SET: 20GA X 8CM 05/25/2018
ARROW INTERNATIONAL INC. ARROW ARTERIAL CATH SET: 20GA X 8CM 05/25/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7FR X 60CM 05/22/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7 FR X 20 CM 05/14/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7 FR X 20 CM 05/14/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 2-LUMEN 7 FR X 20 CM 04/06/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7FR X 60CM 03/22/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 7FR X 16CM 03/14/2018
PENUMBRA, INC. BENCHMARK 6F 071 DELIVERY CATHETER 03/01/2018
ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 8.5FR X 20CM 02/22/2018
-
-