BEUDAMED
    9 results · 19ms · 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 ×

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 20, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 6, 2012

    CONTOUR TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·August 27, 2010

    COMPRESS BOLT CONCENTRIC CLAMP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 13, 2018

    FINN ROTATING HINGE MODULAR FEMORAL/TIBIAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 13, 2018

    RAMIREZ HICO TIBIAL SPINDLE POROUS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 13, 2018

    COMPRESS (TM) PROXIMAL TIBIAL BASE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 13, 2018

    COMPRESS LIGAMENT ANCHOR WASHER WITH SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 13, 2018

    4.3MM CROWE POINT TWIST DRILL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HTW·July 7, 2021