BEUDAMED
    3 results · 18ms · 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 ×

    HERCULITE XRV

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·June 18, 2014

    EON MINI 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 7, 2010

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code DZL·December 20, 2012