• 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: FMF Patient Problem: Fall Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NOVO NORDISK A/S NOVOPEN 01/05/2024
NOVO NORDISK A/S NOVOPEN 6 09/29/2023
NOVO NORDISK A/S NOVOPEN 5 06/27/2022
COMPANION MEDICAL INC INPEN MMT-105NNGYNA NOVO NORDISK GRAY 06/01/2022
ELI LILLY AND COMPANY HUMAPEN ERGO II 04/23/2020
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 01/06/2020
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 09/20/2019
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (UNKNOWN COLOR) 09/18/2019
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN 4 07/31/2019
ELI LILLY AND COMPANY HUMAPEN LUXURA BURGUNDY 06/04/2019
-
-