• 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 
 4 
 
 
40 records meeting your search criteria returned- Product Code: HIH Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HOLOGIC, INC. MYOSURE REACH 10/12/2021
HOLOGIC, INC. MYOSURE TISSUE REMOVAL DEVICE 10/05/2021
HOLOGIC, INC. MYOSURE REACH 06/24/2021
HOLOGIC, INC. MYOSURE TISSUE REMOVAL DEVICE 06/04/2021
COVIDIEN MANSFIELD TRUCLEAR 03/22/2021
COVIDIEN MANSFIELD TRUCLEAR 03/22/2021
COVIDIEN MANSFIELD TRUCLEAR 02/09/2021
HOLOGIC, INC. MYOSURE REACH HYSTEROSCOPIC TISSUE REMOV 10/29/2020
HOLOGIC, INC. MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYS 03/07/2019
HOLOGIC INC. MYOSURE REACH 01/02/2019
-
-