• 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 
 > 
 
17 records meeting your search criteria returned- Product Code: KFM Product Problem: Device Alarm System Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 01/03/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR 10/27/2021
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR 12/21/2020
MAQUET CARDIOPULMONARY GMBH HEART LUNG MACHINE 01/22/2020
GETINGE MAQUET GROUP / MAQUET CARDIOPULM JOSTRA (MAQUET) ROTAFLOW CONSOLE 10/15/2019
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO SARNS DELPHIN BASE ADAPTER WITH BATTERY 11/15/2017
SORIN GROUP DEUTSCHLAND SORIN CENTRIFUGAL PUMP CONSOLE 11/16/2016
TERUMO CARDIOVASCULAR SYSTEMS CORP. SARNS CENTRIFUGAL SYSTEM 09/16/2016
TERUMO CARDIOVASCULAR SYSTEMS CORP. SARNS CENTRIFUGAL SYSTEM 07/06/2016
TERUMO CARDIOVASCULAR SYSTEMS CORP. SARNS CENTRIFUGAL SYSTEM 05/25/2016
-
-