BEUDAMED
    4 results · 15ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·March 18, 2013

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code LXH·March 16, 2011

    THE ELECTRODE STORE

    FDA Adverse Event
    Malfunction ·THE ELECTRODE STORE·Product code GXZ·July 17, 2021

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·April 17, 2025