• 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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
 
246 records meeting your search criteria returned- Product Code: MHY Product Problem: Delayed Charge Time Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/11/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/08/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/06/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/05/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/23/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/09/2020
MEDTRONIC NEUROMODULATION ACTIVA 12/07/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/02/2020
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 11/24/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 11/24/2020
-
-