BEUDAMED
    7 results · 30ms · Sources: EU EUDAMED, US FDA

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    ILIAC CREST BONE MARROW ASPIRATION NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6

    FDA 510(k)
    FDA Class 2 ·Neurology

    Rampart A Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    REVO MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWP·February 9, 2013

    COAGUCHEK® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·January 7, 2011

    PROMUS PREMIER?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 23, 2014