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
 

 
 
7 records meeting your search criteria returned- Product Code: KDI Product Problem: Coagulation in Device or Device Ingredient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BELLCO SRL CLEARUM HS 08/21/2023
BELLCO SRL CLEARUM HS 08/21/2023
OGDEN MANUFACTURING PLANT OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 02/15/2023
BAXTER HEALTHCARE CORPORATION AK 96 MACHINES 02/08/2023
CHF SOLUTIONS, INC. AQUADEX SMARTFLOW CONSOLE 04/16/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 06/09/2020
TERUMO CORPORATION, ASHITAKA CAPIOX HEMOCONCENTRATOR 06/02/2020
-
-