BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    PRIMEDIC DEFIBRILLATORS-N/B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471121928·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 125mm

    SCULPTOR ROBOTIC GUIDANCE ARM (RGA)

    FDA 510(k)
    FDA Class 2 ·Neurology

    CEMENT RESTRICTOR, SMALL AND LARGE

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

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 14, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010

    FLEXTEND

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DTB·July 9, 2014