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 
 > 
 
16 records meeting your search criteria returned- Product Code: KDI Product Problem: Output Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GAMBRO RENAL PRODUCTS, INC. PHOENIX 02/21/2023
GAMBRO RENAL PRODUCTS, INC. PHOENIX 02/21/2023
GAMBRO RENAL PRODUCTS, INC. PHOENIX 02/21/2023
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 12/08/2022
OUTSET MEDICAL, INC. TABLO(R) HEMODIALYSIS SYSTEM 12/06/2022
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 05/07/2022
BAXTER HEALTHCARE PRISMAFLEX HF20 02/22/2022
NXSTAGE MEDICAL, INC. NXSTAGE CARTRIDGE EXPRESS 12/23/2021
GAMBRO INDUSTRIES PRISMAFLEX SET 09/03/2021
BAXTER HEALTHCARE CORPORATION GAMBRO PHOENIX 07/22/2021
-
-