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

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    Filters Regulation: Us FDA ×

    CARDIOLINE touchECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEMORY STAPLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FIBER ONE

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

    SINGLE EXTENSION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 7, 2011

    MICRO SAGITTAL SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·June 10, 2013

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·September 8, 2008