BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    WAKO AUTOKIT LP(A)

    FDA 510(k)
    FDA Class 2 ·Immunology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981446·anteriors; shade BL1; mould BIM6

    BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Bard Power-Injectable Implantable Ports (PowerPorts®)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·February 27, 2013

    SPACEMAKER PREPERITONEAL DIST BALLOON

    FDA Adverse Event
    Malfunction ·USSC PUERTO RICO·Product code GCJ·January 11, 2011

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·July 24, 2014

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018