• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
147 records meeting your search criteria returned- Product Code: DWA Report Date From: 1/1/2020 Report Date To: 12/31/2020

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG 2ND GENERATION PRIMARY CONSOLE 04/16/2020
LIVANOVA DEUTSCHLAND GMBH CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAM 04/15/2020
THORATEC SWITZERLAND GMBH MAG MONITOR 04/15/2020
LIVANOVA DEUTSCHLAND GMBH CENTRIFUGAL PUMP 5 (CP5) 04/10/2020
LIVANOVA DEUTSCHLAND GMBH CENTRIFUGAL PUMP 5 (CP5) 04/09/2020
LIVANOVA DEUTSCHLAND GMBH CENTRIFUGAL PUMP 5 (CP5) 04/09/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO SARNS CENTRIFUGAL SYSTEM 04/08/2020
THORATEC SWITZERLAND GMBH PRIM CONS 1ST GEN, STANDALONE 04/01/2020
PERFUSION SYSTEMS MOTOR EXTERNAL DRIVE 03/20/2020
LIVANOVA DEUTSCHLAND GMBH CENTRIFUGAL PUMP 5 (CP5) 03/19/2020
-
-