Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
93 records meeting your search criteria returned- Product Code: GEI Product Problem: Improper Flow or Infusion Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 2 03/18/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 03/09/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW 6 PRO 03/09/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 02/27/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW 7 XB BISECTOR (US) 02/20/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW 7 XB BISECTOR (US) 02/20/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW 7 XB BISECTOR (US) 02/20/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 2 02/11/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 2 01/17/2020
MAQUET CARDIOVASCULAR LLC VASOVIEWHEMPRO 01/08/2020
-
-