BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    XOD Diathermia Radiofrequency Device

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

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 130

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 14, 2012

    OxyLight 2.0

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

    HEPARINASE HR ACT CONTROL, MODEL 550-12

    FDA 510(k)
    FDA Class 2 ·Hematology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 11, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    3.0MM TI CERVICAL SPINE LOCKING SCREW 16MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code OVE·July 23, 2013

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·November 22, 2010

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·October 11, 2022