BEUDAMED
    3 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 ×

    LD CV EZTRK 2 BP IS1 4542 80CM US

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWP·November 11, 2008

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·September 19, 2011

    SPINE & TRAUMA 3D

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code HAW·July 26, 2013