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

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 
 > 
 
54 records meeting your search criteria returned- Product Code: JDI Patient Problem: Cardiac Arrest Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 10/11/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 08/18/2021
DEPUY INTERNATIONAL LTD - 8010379 C STEM AMT LONG 2 STD OFFSET 08/04/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 02/06/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 12/19/2019
DEPUY ORTHOPAEDICS INC US ARTICUL/EZE BALL 32 +5 BR 09/26/2019
DEPUY ORTHOPAEDICS INC US S-ROM M HEAD 36MM +6 09/10/2019
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 09/10/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 08/29/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 08/29/2019
-
-