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

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    QUICKSCREEN AMPHETINE 500 TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776179724·Berke-Jaeger Lid Plate SS

    SURGISIS NERVE CUFF

    FDA 510(k)
    FDA Class 2 ·Neurology

    OSTEOSYMBIONICS, ST TEMPORALIS IMPLANT

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

    Widex

    FDA UDI
    Widex A/S·05706069812404·Widex EVOKE E-PA (Summer gold ) 330, RC coil

    UNKNOWN_OSTEOSYNTHESIS_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER TRAUMA SELZACH·Product code HWC·October 1, 2014

    MEDICHOICE

    FDA Adverse Event
    Injury ·DALIAN GOODWOOD MEDICAL CARE LTD.·Product code KXF·May 23, 2013

    SIGMA 300 DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code DXY·June 16, 2011

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    VORTEK PERCUTANEOUS NEPHROSTOMY KIT WITH J CATHETER

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code LJE·December 31, 2024