6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
NEUROTENS
FDA 510(k)
FDA Class 2
·Neurology
PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
STICK-GARD SAFETY NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
BD INTROSYTE-N
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.·Product code FOZ·June 11, 2014
PEEK PREVAIL CERVICAL INTERBODY DEVICE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code ODP·January 4, 2013
QUICKFLEX MICRO LV LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010