6 results
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16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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ARROW
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 25, 2023
CODMAN 3000
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 28, 2023
CODMAN 3000
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code LKK·July 20, 2023
DEPUY/CMW 2G
FDA Adverse Event
Injury
·DEPUY CMW - 9610921·Product code LOD·December 27, 2019
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·September 21, 2010
PFC SIG RPF CEM FEM SZ 4 RT
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS1219655·Product code NJL·September 16, 2014