• 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 
 > 
 
30 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CYBERONICS - HOUSTON PULSE GEN MODEL 106 04/19/2024
LIVANOVA USA, INC. PULSE GEN MODEL UNKNOWN 02/09/2024
LIVANOVA USA, INC. PULSE GEN MODEL 106 11/06/2023
LIVANOVA USA, INC. PULSE GEN MODEL 104 10/24/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 1000 08/25/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 1000 07/10/2023
CYBERONICS - HOUSTON LEAD MODEL 302 06/16/2023
LIVANOVA USA, INC. PULSE GEN MODEL UNK 06/09/2023
LIVANOVA USA, INC. PULSE GEN MODEL 103 05/05/2023
LIVANOVA USA, INC. LEAD MODEL 304 04/21/2023
-
-