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

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    Filters Regulation: Us FDA ×

    MODEL 900GE1500 HEAD/NECK COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    RED, WHITE & BLUE

    FDA 510(k)
    FDA Class 2 ·Dental

    GH DISPOSABLE AND GH REUSABLE BLOOD PRESSURE CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 16, 2013

    VIBRANT SOUNDBRIDGE

    FDA Adverse Event
    Injury ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·December 23, 2010

    TA 60-3.5 SINGLE USE RELOADABLE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC·Product code GDW·July 8, 2014

    EVOLUT FX DCS

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NPT·November 4, 2025