Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
111 records meeting your search criteria returned- Product Code: DTZ Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CORP., ASHITAKA FX OXY W/HR AND ART FILTER 05/13/2014
TERUMO CORP. ASHITAKA FX OXY W/HR AND ART FILTER 05/06/2014
TERUMO CORPORATION, ASHITAKA FX OXY W/HR 7 ART FILTER 04/30/2014
TERUMO CORP, ASHITAKA FX OXY W/HR & ART FILTER 04/25/2014
TERUMO CORP, ASHITAKA HOLLOW FIBER OXY WITH 4000 ML 04/25/2014
TERUMO CORP, ASHITAKA CAPIOX RX25 OXYGENATOR EAST 04/25/2014
TERUMO CORP, ASHITAKA FX OXY W/HR & ART FILTER 04/25/2014
TERUMO CORP, ASHITAKA BABY FX OXY W/HR & ART FILTER 04/25/2014
TERUMO CARDIOVASCULAR SYSTEMS CORP. SX OXYGENATORY W/ HR X COATING 04/25/2014
TERUMO CORP, ASHITAKA FX OXY W/HR & ART FILTER 04/25/2014
-
-