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

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    CORDIS ANCOR ACTIVE FIXATION LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707063810·TUBE MIM 22/18/45 OCC T-10 R+8 U/R

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707057468·DB TUBE MIM 22/18/45 OCC T-10 R+8 U/R

    PALS PLATINUM NEUROSTIMULATION ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    EUSOL-C

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 14, 2012

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 27, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2015