• 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 
 > 
 
33 records meeting your search criteria returned- Product Code: KDI Patient Problem: Reaction Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 01/28/2021
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH UNKNOWN- DIALYZER 12/31/2020
BAXTER HEALTHCARE CORPORATION REVACLEAR 300 12/21/2020
BAXTER HEALTHCARE CORPORATION THERANOVA 400 11/24/2020
BAXTER HEALTHCARE CORPORATION REVACLEAR 3000 11/23/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 07/29/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 07/29/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 07/17/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 07/14/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 07/14/2020
-
-