3 results
·
18ms
·
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·July 7, 2015
BUCKY DIAGNOST TH
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS GMBH DMC·Product code KPR·February 6, 2014
POLYAXIAL PEDICLE SCREW
FDA Adverse Event
Injury
·ZIMMER SPINE, INC.·Product code NKB·December 27, 2012