• 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 
 6 
 7 
 8 
 > 
 
74 records meeting your search criteria returned- Product Code: DTZ Product Problem: Material Deformation Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 08/23/2024
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 08/21/2024
PERFUSION SYSTEMS FUSION HFO CORTIVA COATED 07/15/2024
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 06/20/2024
TERUMO MEDICAL CORPORATION CAPIOX FX OXYGENATOR 06/19/2024
TERUMO MEDICAL CORPORATION CAPIOX FX25 HOLLOW FIBER OXYGENATOR AF 04/18/2024
TERUMO MEDICAL CORPORATION CAPIOX HOLLOW FIBER OXYGENATOR/ ARTERIAL 03/08/2024
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 02/07/2024
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 12/20/2023
PERFUSION SYSTEMS AFFINITY NT BALANCE 12/20/2023
-
-