BEUDAMED
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    Filters Status: Malfunction ×

    ASSURE WEARABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·KESTRA MEDICAL TECHNOLOGIES, INC.·Product code MVK·December 30, 2025

    DRIVE SHAFT-MINIMUM 520 MM LENGTH-FOR USE WITH

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·February 28, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·March 1, 2011