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

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    B-D/BFI MAIL DISPOSAL SERVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Curiteva Porous PEEK Laminoplasty System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BP 5000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 21, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 30, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014

    EVOLUT FX VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·March 10, 2026

    EVOLUT FX VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·March 10, 2026