6 results
·
22ms
·
Sources: EU EUDAMED, US FDA
LAS-R HUMAN PREALBUMIN TEST
FDA 510(k)
FDA Class 1
·Immunology
SCOUTPRO 8F, 7F AND SLITTER TOOL ADVANCED
FDA 510(k)
FDA Class 2
·Cardiovascular
Patient Status Engine
FDA 510(k)
FDA Class 2
·Cardiovascular
RETRO FEM CONNECTING BOLT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LXH·April 25, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·October 2, 2012
ARTICUL/EZE M 36MM +5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code JDI·July 23, 2010