5 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
S-ROM M HEAD 36MM +3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 2, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 23, 2012
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 13, 2010
INJ. OPTIV DH, W/OEM
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM·Product code IZQ·October 24, 2024
INJ. OPTIV DH, W/OEM
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM·Product code IZQ·April 9, 2024