BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·October 15, 2012

    SOLETRA

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MHY·May 5, 2014

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 6, 2010