BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 12, 2024

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 8, 2011

    BROVIAC

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code FOZ·November 4, 2014

    PEDICSCR MATRIX 5.5 POLYAXIAL Ø5 PREASSM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·July 29, 2013