5 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TESS GLENOID REVERSE HEAD DIAMETER 36
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016
PINN SECTOR HA ACET CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 8, 2013
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 6, 2011
MEDFUSION 2010H SYRINGE INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code FRN·April 25, 2008
THE ELECTRODE STORE
FDA Adverse Event
Malfunction
·THE ELECTRODE STORE·Product code GXZ·July 17, 2021