• 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 
 8 
 9 
 10 
 > 
 
215 records meeting your search criteria returned- Product Code: DTZ Product Problem: Use of Device Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX15REC W/3L RES 01/10/2024
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 10/24/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 10/24/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 3L RES 10/06/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 3L RES 10/06/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX15RWC W/ 3L RES 10/06/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25RWC W/ RES 10/05/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 09/12/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 08/31/2023
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO NS FX25REC W/RES 08/28/2023
-
-