• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: DQO Patient Problem: Blood Loss Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 05/15/2020
MERIT MEDICAL SYSTEMS, INC. IMPRESS BRAIDED PERIPHERAL CATHETER 04/09/2020
TERUMO CORPORATION, ASHITAKA OPTITORQUE ANGIOGRAPHIC CATHETER 12/04/2019
TERUMO CORPORATION, ASHITAKA OPTITORQUE ANGIOGRAPHIC CATHETER 12/04/2019
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 10/28/2019
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 10/28/2019
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 08/08/2017
COOK INC SINGLE LUMEN DISTAL AORTIC PRESSURE MONI 06/06/2017
COOK INC SINGLE LUMEN DISTAL AORTIC PRESSURE MONI 09/12/2016
ICU MEDICAL, INC. CONTRAST MEDIA INJECTION LINE 12/30/2015
-
-