• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
99 records meeting your search criteria returned- Product Code: HIH Product Problem: Material Fragmentation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN MANSFIELD TRUCLEAR 12/01/2020
COVIDIEN MANSFIELD TRUCLEAR 11/30/2020
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR 11/20/2020
RICHARD WOLF GMBH PANOVIEW PLUS 11/10/2020
COVIDIEN MANSFIELD TRUCLEAR 09/01/2020
KARL STORZ SE & CO. KG INNER TUBE FOR 26050SL 08/20/2020
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR 08/19/2020
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 24 FR. 07/28/2020
HOLOGIC, INC. MYOSURE REACH TISSUE REMOVAL DEVICE 05/29/2020
HOLOGIC, INC. MYOSURE REACH TISSUE REMOVAL DEVICE 05/20/2020
-
-