6 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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REPLY
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·November 18, 2010
SM104 MSERIES W5TH WHLOBS3/07
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·January 25, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 11, 2014
ECLIPSE CAGE SCREW S, 30MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·June 16, 2025
ARTHREX ECLIPSE HUMERAL HEAD, 47/18
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·June 16, 2025
UNIVERSAL GLENOID - INLAY MEDIUM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·June 16, 2025