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
 

 
 
8 records meeting your search criteria returned- Product Code: DRS Product Problem: Failure to Reset Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ICU MEDICAL, INC. MONITORING KIT W/ NEEDLELESS VALVE 07/26/2016
ICU MEDICAL, INC. MONITORING KIT W/ NEEDLELESS VALVE 07/26/2016
ICU MEDICAL, INC. SINGLE LINE TRANSPAC IV MONITORING KIT W 06/09/2016
ICU MEDICAL, INC. MONITORING KIT W/ NEEDLELESS VALVE 04/12/2016
ICU MEDICAL, INC. MONITORING KIT W/ NEEDLELESS VALVE 04/11/2016
ICU MEDICAL, INC. TRIFURCATED TRANSPAC IV MONITORING KIT 05/08/2015
ICU MEDICAL, INC. SAFESET TRANSPAC IV MONITORING KITS 04/28/2014
NAVILYST MEDICAL NAMIC 01/28/2014
-
-