• 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 
 > 
 
17 records meeting your search criteria returned- Product Code: NTE Patient Problem: Hematoma Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN SPIDER FX 09/19/2022
INVATEC SPA MO.MA ULTRA 06/21/2022
COVIDIEN SPIDER FX 04/13/2022
COVIDIEN SPIDER FX 12/09/2021
COVIDIEN SPIDER FX 10/05/2021
COVIDIEN SPIDER FX 07/29/2021
COVIDIEN SPIDER RX 06/21/2021
COVIDIEN SPIDER FX 10/30/2020
COVIDIEN SPIDER FX 10/28/2020
COVIDIEN SPIDER FX 10/19/2020
-
-