BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    TECHNOMED PULSOLITH LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODEL 435-04 CARDIFIX SIDE HOOK IMPLANT. PACE LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    DIATRON BLOOD GLUCOSE METER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PWRD ECHELON LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 25, 2014

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·January 3, 2013

    UNKNOWN DEPUY DURALOC CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·November 8, 2010