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

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 
 > 
 
13 records meeting your search criteria returned- Product Code: KDI Patient Problem: Respiratory Failure Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 10/25/2022
CONCORD MANUFACTURING 2008T HD SYS. CDX W/BIBAG BLUE STAR 01/31/2022
CONCORD MANUFACTURING 2008T MACHINE 10/15/2021
OUTSET MEDICAL, INC. TABLO HEMODIALYSIS SYSTEM 01/05/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 08/21/2020
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYS., WITH CDX 07/29/2020
CONCORD MANUFACTURING 2008T MACHINE 06/23/2020
GAMBRO AB PRISMAFLEX 03/18/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 11/27/2019
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX M100 09/06/2019
-
-