BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    GYROSCAN T5 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

    FDA 510(k)
    FDA Class 2 ·Radiology

    IntelliCartTM System

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

    COMPOSITE RESTORATIVE, PASTE/PASTE TYPE

    FDA 510(k)
    FDA Class 2 ·Dental

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code NVY·January 13, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·November 1, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 21, 2012

    CORAIL AMT SZ10 135 LOW N COL

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS 3003895575·Product code LZO·July 19, 2019