BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    THE S.A.F.E. SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SMARTSPOT PRIMAX

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPP TERMINAL DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    TRILOGY 202

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·April 9, 2014

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    FDA Adverse Event
    MEDLINE·Product code GDY·November 16, 2012

    MERIT MANIFOLD

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·October 4, 2010

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023