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

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    SpineAR SNAP (SyncAR Spine)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Narval Brux

    FDA 510(k)
    FDA Unclassified ·Unknown

    StentBoost Mobile

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERLING?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·November 11, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 24, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2013

    Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm, Sterile EO, Rx Only, Quantity 1, UDI: 07613327376067

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·February 3, 2021

    ACCOLADE DR SL MRI (Model L311)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025