• 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 
 > 
 
208 records meeting your search criteria returned- Product Code: DTZ Product Problem: Infusion or Flow Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH OXYGENATOR 01/22/2021
TERUMO CORPORATION, ASHITAKA CAPIOX RX25 OXYGENATOR 01/14/2021
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR 12/23/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 12/21/2020
MAQUET CARDIOPULMONARY GMBH OXYGENATOR 12/15/2020
TERUMO CORPORATION, ASHITAKA CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL 11/23/2020
TERUMO CORPORATION, ASHITAKA CAPIOX CUSTOM PACK 11/19/2020
TERUMO CORPORATION, ASHITAKA CAPIOX CUSTOM PACK 11/11/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 4L RES 11/03/2020
EUROSETS S.R.L. ADVANCED MEMBRANE GAS EXCHANGE PMP STERI 10/27/2020
-
-