8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Vital Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
ARTICUL/EZE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295129011·ARTICUL/EZE TRIAL BALL GROOVED 32mm DIA +9
FIRMap Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
KALIX II IMPLANT, MODEL 141 0XX WITH XX
FDA 510(k)
FDA Class 2
·Orthopedic
LONG NAIL KIT R1.5, TI, RIGHT GAMMA3 10X260MM X 1
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·August 28, 2012
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 5, 2008
TOTALCARE BARIATRIC PLUS
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·August 31, 2011
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·July 29, 2013