• 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 
 7 
 > 
 
62 records meeting your search criteria returned- Product Code: DTZ Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 02/22/2024
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR 07/13/2022
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 03/01/2022
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR 02/14/2022
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 10/01/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 10/01/2021
TERUMO CORPORATION, ASHITAKA CAPIOX CUSTOM PACK 10/01/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 10/01/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 09/28/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR 07/20/2021
-
-