8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PREAMPLIFIER MODULE, EKG RESPIRATION
FDA 510(k)
FDA Class 2
·Anesthesiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189374·AK3 Femoral Distal Locating Device, 4° Bushing
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011790304000·topic Bracket with hook, - 2° Torque, + 13° Ang...
Kingon P2 Oxygen Concentrator
FDA 510(k)
FDA Class 2
·Anesthesiology
WAVEON WRX BONE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BUILD-IT FR
FDA Adverse Event
Injury
·PENTRON CLINICAL·Product code EBF·May 5, 2014
RELIA DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NVZ·October 15, 2012
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·August 6, 2010