• 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 
 5 
 6 
 7 
 8 
 9 
 > 
 
82 records meeting your search criteria returned- Product Code: LNH Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
FUJIFILM HEALTHCARE CORPORATION OASIS XP 1.2T OPEN MRI SYSTEM 06/30/2022
FUJIFILM HEALTHCARE CORPORATION ALTAIRE MRI SYSTEM 06/28/2022
FUJIFILM HEALTHCARE CORPORATION OASIS XP 1.2T OPEN MRI SYSTEM 06/28/2022
GE MEDICAL SYSTEMS, LLC SIGNA PIONEER 06/23/2022
SIEMENS AG/SIEMENS HEALTHCARE GMBH SIEMENS ESPREE 05/13/2022
GE MEDICAL SYSTEMS, LLC. GE MRI 04/22/2022
PHILIPS NORTH AMERICA LLC. PHILIPS INNGENIA 3T MRI 04/14/2022
PHILIPS ELECTRONICS NEDERLAND B.V. INGENIA ELITION X 04/05/2022
Unknown Manufacturer MRI 04/04/2022
FUJIFILM HEALTHCARE CORPORATION ALTAIRE MR SYSTEM 03/08/2022
-
-