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 Patient Problem: Cramp(s) Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIKKISO CO.,LTD DBB-06 HEMODIALYSIS DELIVERY SYSTEM 12/10/2020
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYS., WITH CDX 09/18/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 05/27/2020
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYSTEM W/BIBAG 03/31/2020
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYSTEM W/BIBAG 12/27/2019
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS OLC/DP, SPANISH 10/07/2019
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 05/30/2019
-
-