BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    P POLYMER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KTP/532 & KTP/YAG

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

    Proteus XR/a (SlOK : K993090)

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code KPR·August 9, 2019

    LEFT 16MM VARIABLE ANGLE SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·February 27, 2013

    SEGURA HEMISPHERE STONE RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·February 16, 2011

    HUDSON PEDIATRIC BREATHING CIRCUIT, 30"

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code OFP·July 24, 2014

    Proteus XR/a (SlOK : K993090)

    FDA Enforcement
    Class II ·Ongoing·GE Healthcare, LLC·October 2, 2019