3 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014
HIP SCR Ø6.5 SELF-TAP L75 F/EXPERT LFN T
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HSB·November 7, 2012
PINN CAN BONE SCREW 6.5MMX20MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code NDJ·August 27, 2010