• 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 
 > 
 
58 records meeting your search criteria returned- Product Code: DTZ Product Problem: Disconnection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO PRESCRIPTIVE OXY PACK - CAPIOX 11/22/2019
MAQUET CARDIOPULMONARY GMBH OXYGENATOR WITH INTEGRATED HEAT EXCHANGE 05/03/2019
SORIN GROUP ITALIA S.R.L. INSPIRE 6F HOLLOW FIBER OXY W/ INTEGRATE 05/09/2018
SORIN GROUP ITALIA S.R.L. INSPIRE 6F HOLLOW FIBER OXY W/ INTEGRATE 04/27/2018
TERUMO CARDIOVASCULAR SYSTEMS PRESCRIPTIVE OXY PACK - CAPIOX 11/17/2017
TERUMO MEDICAL CORP. CAPIOX 10/03/2017
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 07/23/2017
TERUMO CARDIOVASCULAR SYSTEMS CORP. STERILE FX25RWC W/ RES 05/11/2017
TERUMO CORPORATION, ASHITAKA CAPIOX RX OXYGENATOR 04/06/2017
TERUMO CARDIOVASCULAR SYSTEMS CORP. NS FX25RWC W/RES 02/20/2017
-
-