7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ISLAM BONE MARROW BIOPSY NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PressON™
FDA UDI
NEXUS SPINE, L.L.C.·B6788203390·Wand Calipers
PROCOLL
FDA 510(k)
FDA Unclassified
·Unknown
DORNIER DIODE LASER FAMILY MEDILAS D, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·May 20, 2014
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code MMH·November 6, 2012
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·August 30, 2010