• 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 
 > 
 
33 records meeting your search criteria returned- Product Code: JCX Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER INSTRUMENTS NEPTUNE 03/31/2023
STRYKER INSTRUMENTS NEPTUNE 03/31/2023
STRYKER CORPORATION NEPTUNE 3 WASTE MANAGEMENT 09/29/2022
ZIMMER BIOMET INTELLICART / ZIMMER SURGI ZIMMER WASTE DISPOSAL UNIT 03/25/2022
ZIMMER BIOMET INTELLICART / ZIMMER SURGI ZIMMER WASTE DISPOSAL UNIT 03/25/2022
ZIMMER BIOMET INTELLICART / ZIMMER SURGI ZIMMER WASTE DISPOSAL UNIT 03/25/2022
ZIMMER BIOMET INTELLICART / ZIMMER SURGI ZIMMER BIOMET INTELLICART WASTE DISPOSAL 03/25/2022
ZIMMER BIOMET INTELLICART / ZIMMER SURGI ZIMMER BIOMET INTELLICART WASTE DISPOSAL 03/25/2022
ZIMMER SURGICAL, INC. INTELLICART 03/16/2022
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, IN INTELLICART¿ 11/15/2021
-
-