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

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    MODUMED MUGE

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Zimmer, Inc.·00889024133334·

    NA

    FDA UDI
    Zimmer, Inc.·00889024133341·

    POWDERLITE

    FDA 510(k)
    FDA Class 2 ·Dental

    Intracept Intraosseous Nerve Ablation System (component Intracept RF Probe)

    FDA 510(k)
    FDA Class 2 ·Neurology

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 5, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·December 3, 2013

    UNKNOWN ZIMMER HARRIS-GALLANTE HIP

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·May 14, 2015