BEUDAMED
    6 results · 21ms · 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 ×

    PREMISE COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·April 24, 2015

    PREMISE COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·April 24, 2015

    PREMISE COMPOSITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·April 24, 2015

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 14, 2013

    SYNCHRON® LX20 CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 15, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 28, 2014