BEUDAMED
    4 results · 27ms · 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 ×

    BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012

    OXIMAX N-560 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·PEDIANA·Product code DQA·April 29, 2014

    SWARTZ BRAIDED TRANS. GUIDING INT., 8F, SLO

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DYB·February 1, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·January 26, 2011