BEUDAMED
    3 results · 29ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    M2A MAGNUM MODULAR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 10, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 8, 2014

    SIMPLEX P - CE TOBRA FD 10-PK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·December 17, 2012