BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    DARWIN KNEE SYSTEM (TC3)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701121·BASE Ti HL Implant, 8x38x28mm 30°

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 28, 2024

    K3

    FDA 510(k)
    FDA Class 1 ·Dental

    SPORTMESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

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

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·July 23, 2014

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 7, 2011