9 results
·
28ms
·
Sources: EU EUDAMED, US FDA
ESCORT 300 SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909116652·REVELATION DIAMOND 368-023F - 5 PACK
SONON Ultrasound Imaging System, Model: SONON300C
FDA 510(k)
FDA Class 2
·Radiology
BCT SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETE·Product code LZG·May 28, 2014
ANIMAS INSULIN CARTRIDGE
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·January 11, 2013
MAVERICK2 BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LOX·December 1, 2010
SEE H10
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018
TDx/TDxFLx Cortisol Reagent Pack, list 9116-65; Abbott Laboratories, Diagnostics Division, Abbott Park, IL 60064
FDA Recall
Terminated
·Abbott Laboratories HPD/ADD/GPRD·Product code JFT·February 16, 2004