BEUDAMED
    5 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 ×

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·October 26, 2021

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·October 26, 2021

    SINGLE LUMEN PERIPHERALLY INSERTED CENTER VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code FOZ·May 1, 2014

    OLYMPUS VISERA LAPARO-THORACO VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GCJ·October 9, 2012

    PRECISION XTRA/OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·September 28, 2007