BEUDAMED
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    Filters Status: Malfunction ×

    LIGATING DEVICE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GEI·June 6, 2014

    CE INTERMATE SV 100, 48 PACK,50125

    FDA Adverse Event
    Malfunction ·Product code FRN·January 28, 2011

    NUVASIVE HELIX ACP SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code KWQ·June 1, 2022