BEUDAMED
    8 results · 33ms · 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: Other ×

    CERRETOM NL3000

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·June 18, 2014

    CERETOM NL-3000

    FDA Adverse Event
    Other ·NEUROLOGICA, CORPORATION·Product code JAK·May 31, 2012

    CERETOM (TRANSFER SCAN BOARD)

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·November 12, 2008

    CERETOM NL3000

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·February 14, 2014

    CERETOM NL3000

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·February 14, 2014

    CERETOM NL3000

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·February 14, 2014

    CERETOM

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·January 24, 2007

    CERETOM (TRANSFER SCAN BOARD)

    FDA Adverse Event
    Other ·NEUROLOGICA CORPORATION·Product code JAK·February 13, 2009