• 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
 

 
 
9 records meeting your search criteria returned- Product Code: IDP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1860UV 02/04/2022
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1950 03/19/2020
LEICA BIOSYSTEMS NUSSLOCH LEICA CM1950 01/18/2019
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1950 01/18/2019
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1950 06/27/2017
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1520 12/02/2016
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1850 01/21/2016
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1850 01/20/2016
LEICA BIOSYSTEMS NUSSLOCH GMBH LEICA CM1850UV 05/16/2014
-
-