• 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 
 > 
 
53 records meeting your search criteria returned- Product Code: DTZ Product Problem: Insufficient Flow or Under Infusion Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH OXYGENATOR 11/30/2023
MAQUET CARDIOPULMONARY GMBH HLS SET ADVANCED 04/25/2023
JULIA KAPFENBERGER HLS SET ADVANCED 04/24/2023
TERUMO CORPORATION, ASHITAKA CAPIOX RX25 OXYGENATOR 11/23/2022
MAQUET CARDIOPULMONARY GMBH HLS SET ADVANCED 04/07/2022
MAQUET CARDIOPULMONARY GMBH HLS SET ADVANCED 04/07/2022
MAQUET CARDIOPULMONARY GMBH HLS SET ADVANCED 03/30/2022
CARDIACASSIST INC. TANDEMLUNG OXYGENATOR 01/12/2022
TERUMO CORPORATION, ASHITAKA CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL 11/19/2021
TERUMO CORPORATION, ASHITAKA CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL 11/19/2021
-
-