BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    CARDIAC REVIEW STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7402812515·Rampart-O

    PENCAN®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code BSP·May 6, 2025

    BIFURCATED VACCINATING NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PENCAN SPINAL NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2014

    CONSULTA CRT-P

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·August 16, 2010

    PENCAN®

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code BSP·April 10, 2025