BEUDAMED
    6 results · 28ms · 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 ×

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·June 23, 2025

    MEDTRONIC

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011

    VISTA BASIC - IFVB

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·July 8, 2014

    T2 - NAIL HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025