• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
439 records meeting your search criteria returned- Product Code: FMF Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 07/02/2018
ELI LILLY AND COMPANY HUMAPEN, UNKNOWN DEVICE 06/26/2018
BD MEDICAL - DIABETES CARE BD INSULIN SYRINGE WITH THE BD ULTRA-FIN 06/25/2018
BD MEDICAL - DIABETES CARE BD ULTRA-FINE¿ INSULIN SYRINGE 06/21/2018
BD MEDICAL - DIABETES CARE BD¿ INSULIN SYRINGE WITH NEEDLE 06/18/2018
BECTON DICKINSON MEDICAL (SINGAPORE) BD PLASTIPAK¿ SYRINGE, LUER-LOK¿ 06/14/2018
BECTON DICKINSON, S.A. BD PLASTIPAK¿ CONCENTRIC LUER LOCK SYRI 06/14/2018
BECTON DICKINSON MEDICAL SYSTEMS BD PLASTIC NON-STERILE LUER-LOK¿ TIP SYR 06/11/2018
BECTON DICKINSON, S.A. BD PLASTIPAK¿ LUER-LOK¿ SYRINGE 06/11/2018
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 06/08/2018
-
-