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 
 
 
11 records meeting your search criteria returned- Product Code: DWF Product Problem: Device Markings/Labelling Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA 02/24/2023
EDWARDS LIFESCIENCES AVID THIN-FLEX DUAL STAGE 29/37F VENOUS 02/03/2023
BARD PERIPHERAL VASCULAR, INC. CAROTID BYPASS SHUNT 06/06/2022
BARD PERIPHERAL VASCULAR, INC. CAROTID BYPASS SHUNT 06/03/2022
MEDTRONIC MEXICO S. DE R.L. DE CV BIO-MEDICUS STANDARD INSERTION KIT 09/10/2021
MEDTRONIC MEXICO S. DE R.L. DE CV BIO-MEDICUS STANDARD INSERTION KIT 09/10/2021
SORIN GROUP ITALIA SRL MODIFIED STOCKERT-SHILEY VENOUS CATHETER 05/26/2021
LIVANOVA USA INC THORACIC CATHETER 04/03/2019
LIVANOVA USA INC THORACIC CATHETER 04/03/2019
ORIGEN BIOMEDICAL, INC ORIGEN REINFORCED DUAL LUMEN CATHETER 04/02/2019
-
-