BEUDAMED
    4 results · 27ms · 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 ×

    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

    COBE MONITOR LINE

    FDA Adverse Event
    Injury ·SORIN CO·Product code DWF·February 23, 2008