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

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    VERIFY(R) REFERENCE PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cartiva SCI Disposable Instrumentation Set

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 13, 2020

    CARTIVA IMPLANT

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·November 9, 2020

    PINN MAR +4 10D 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 18, 2014

    QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·October 7, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LWS·December 17, 2012