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 
 > 
 
37 records meeting your search criteria returned- Product Code: DSP Product Problem: Entrapment of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DATASCOPE MAHWAH CARDIOSAVE 08/24/2017
ARROW INTERNATIONAL INC. FIBEROPTIX ULTRA 8 IAB: 8FR 40CC 08/10/2017
MAQUET IABP BALLOON 03/06/2017
DATASCOPE FAIRFIELD SENSATION PLUS 7.5FR. 40CC IAB 12/30/2016
ARROW INTERNATIONAL INC. NARROWFLEX IAB: 8FR 30CC 11/17/2016
ARROW INTERNATIONAL INC. CARDIAC UNKNOWN MATERIAL 08/03/2016
ARROW INTERNATIONAL INC. FIBEROPTIX ULTRA 8 IAB: 8FR 40CC 05/09/2016
ARROW INTERNATIONAL INC. IAB : 8 FR - 40 CC FOS 09/14/2015
ARROW INTERNATIONAL INC. IAB : 7.5 FR - 40 CC 07/13/2015
ARROW INTL., INC. IAB 8 FR - 40 CC FOS 04/27/2015
-
-