BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    ELECTROSURGICAL DEVICE, CUTTING AND COAGULATION AND ACCESSORIES

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

    MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    PALADUR

    FDA 510(k)
    FDA Class 2 ·Dental

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·December 28, 2010

    M2A-MAGNUM MODULAR HEAD SZ 44MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 6, 2013

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 21, 2014