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
 

 
 
9 records meeting your search criteria returned- Product Code: KSR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO BCT, LTD REVEOS AUTOMATED WHOLE BLOOD PROCESSING 01/16/2024
TERUMO BCT REVEOS 01/04/2024
TERUMO BCT REVEOS AUTOMATED WHOLE BLOOD PROCESSING 12/28/2023
TERUMO BCT REVEOS AUTOMATED WHOLE BLOOD PROCESSING 12/27/2023
TERUMO BCT IMUGARD WB PLT PLATELET POOLING SET 12/21/2023
TERUMO CORPORATION TERUFLEX 12/29/2020
TERUMO BCT, LTD TERUFLEX BLOOD BAG SYSTEM 04/02/2019
DEROYAL INTERCONTINENTAL, S.R.L. UMBILICUP 10/05/2018
MILTENYI BIOTEC CLINIMACS 09/22/2014
-
-