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 
 5 
 > 
 
43 records meeting your search criteria returned- Product Code: DSP Product Problem: No Audible Alarm Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARROW INTERNATIONAL LLC ULTRAFLEX IAB: 7.5FR 30CC 07/17/2024
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 06/14/2024
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE G PLUG 05/07/2024
ARROW INTERNATIONAL LLC AC3 OPTIMUS IABP NA/EMEA 01/02/2024
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 07/31/2023
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 11/29/2022
ARROW INTERNATIONAL, LLC (SUBSIDIARY OF IABP 07/26/2022
DATASCOPE CORP. - MAHWAH UNKNOWN CARDIOSAVE INTRA-AORTIC BALLOON 04/12/2022
DATASCOPE CORP. - MAHWAH CARDIOSAVE HYBRID, TYPE B PLUG 02/08/2022
ARROW INTERNATIONAL INC. AC3 OPTIMUS IABP NA/EMEA 09/23/2021
-
-