BEUDAMED
    3 results · 13ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 1, 2013

    KAPPA 900 SR

    FDA Adverse Event
    Injury ·EOC HEERLEN DISTRIBUTION CTR·Product code DXY·August 8, 2014