BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    DESCRIBE PFD Patch

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

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10887488270043·STERILE CERVICAL TRAY

    SYNTHES STERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONVENTUS ORTHOPAEDICS FRACTURE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 17, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·July 20, 2011

    TRIAGE CARDIAC PANEL

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code MMI·September 20, 2008

    PANTHER FUSION ADV/HMPV/RV ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC INCORPORATED·Product code OCC·October 12, 2021