• 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: IZI Product Problem: Failure to Power Up Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 05/09/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10/10 05/01/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 03/29/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 01/30/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 01/09/2023
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD 12/30/2022
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10/10 11/29/2022
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10 11/14/2022
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10 10/06/2022
-
-