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

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
 

 
 
10 records meeting your search criteria returned- Product Code: FMF Patient Problem: Weight Changes Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 07/23/2020
ELI LILLY AND COMPANY HUMAPEN ERGO II 07/08/2020
ELI LILLY AND COMPANY HUMAPEN ERGO II 10/08/2019
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (GRAPHITE) 08/14/2019
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (PINK) 07/03/2019
ELI LILLY AND COMPANY HUMAPEN ERGO II 11/20/2018
ELI LILLY AND COMPANY HUMAPEN ERGO II 11/02/2018
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 09/10/2018
ELI LILLY AND COMPANY HUMAPEN LUXURA CHAMPAGNE 05/25/2018
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 03/01/2018
-
-