• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
418 records meeting your search criteria returned- Product Code: LWS Product Problem: Protective Measures Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC EUROPE SARL EVERA¿ XT VR 05/28/2020
MEDTRONIC MED REL MEDTRONIC PUERTO RICO PROTECTA XT VR 05/19/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 05/11/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA¿ S VR 05/11/2020
MEDTRONIC EUROPE SARL MAXIMO II DR 05/06/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 04/15/2020
MEDTRONIC MED REL MEDTRONIC PUERTO RICO VIRTUOSO II DR 04/06/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. VISIA AF XT VR 03/22/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT VR SURESCAN 03/11/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA¿ XT DR 03/11/2020
-
-