BEUDAMED
    5 results · 14ms · 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 Status: Malfunction ×

    HL20 BUBBLE SENSOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 30, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 9, 2013

    BD SAFE-CLIP¿ NEEDLE CLIPPING & STORAGE DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·September 25, 2019

    SHARPS DISPOSAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·August 16, 2019