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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 > 
 
70 records meeting your search criteria returned- Product Code: DSP Product Problem: Failure of Device to Self-Test Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DATASCOPE CORP. - MAHWAH CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH 02/21/2023
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 12/19/2022
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 11/30/2022
DATASCOPE CORP. - MAHWAH CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH 03/23/2022
DATASCOPE CORP. CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH 02/07/2022
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID TYPE B PLUG 11/22/2021
DATASCOPE CORP. - MAHWAH CS300 04/05/2019
DATASCOPE CORP. - MAHWAH CS300 04/03/2019
DATASCOPE CORP. - MAHWAH CS300 03/29/2019
DATASCOPE CORP. - MAHWAH CS300 03/25/2019
-
-