• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
249 records meeting your search criteria returned- Product Code: MCW Product Problem: Material Deformation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND TURBOHAWK PLUS 6FR 01/19/2024
MEDTRONIC IRELAND TURBOHAWK PLUS 6FR 01/18/2024
MEDTRONIC IRELAND HAWKONE 7FR 01/10/2024
MEDTRONIC IRELAND HAWKONE 6FR 01/02/2024
UNKNOWN ROTAREX 01/02/2024
MEDTRONIC IRELAND HAWKONE 6FR 12/18/2023
MEDTRONIC IRELAND HAWKONE 6FR 12/13/2023
SPECTRANETICS CORPORATION TURBO-ELITE LASER ATHERECTOMY CATHETER 12/01/2023
UNKNOWN ROTAREX 11/30/2023
MEDTRONIC IRELAND TURBOHAWK PLUS 6FR 11/17/2023
-
-