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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
327 records meeting your search criteria returned- Product Code: DTZ Report Date From: 1/1/2018 Report Date To: 12/31/2018

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO PRESCRIPTIVE OXY PACK - CAPIOX 11/19/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX15 11/16/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX OXYGENATOR 11/16/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 4L RES 11/15/2018
SORIN GROUP ITALIA S.R.L. D101 KIDS INFANT HOLLOW FIBER MEMBRANE O 11/15/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO HOLLOW FIBER OXY WITH 3000 ML 11/12/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 11/12/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 11/12/2018
TERUMO CORPORATION, ASHITAKA CAPIOX FX15 11/12/2018
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 11/05/2018
-
-