3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013
OCTRODE PERCUTANEOUS LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·December 7, 2010
RECAP CEMENT FMRL HD RESUR 50M
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 9, 2014