3 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
POWERFLEX P3 PTA DILATATION CATHETER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code LIT·August 24, 2011
ALTRX +4 10D 36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 11, 2013
SMR REVERSE HUMERAL BODY SHORT
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code PHX·May 14, 2024