• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
55 records meeting your search criteria returned- Product Code: BSZ Product Problem: Failure of Device to Self-Test Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DATEX-OHMEDA, INC. CARESTATION 620 12/27/2018
GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUX CARESTATION 650 A1 12/17/2018
DATEX-OHMEDA, INC. AISYS CS2 12/17/2018
DATEX-OHMEDA, INC. AVANCE CS2 11/20/2018
DATEX-OHMEDA, INC. AISYS 11/20/2018
DATEX-OHMEDA, INC. AISYS 11/07/2018
DATEX-OHMEDA, INC. AVANCE CS2 11/06/2018
GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUX CARESTATION 620 10/29/2018
GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUX CARESTATION 620 07/27/2018
GE HEALTHCARE FINLAND OY ADU 07/07/2018
-
-