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

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    REVISED BATTERY CHARGER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SignalMark Breast Marker

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

    QUADROX-I SMALL ADULT WITH AND WITHOUT INTERGRATED ARTERIAL FILTER WITH SOFTLINE COATING, MODELS HMO 50000, HMO 51000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PFC*SIGMA/RD/DOME PAT 3PEG,35

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 6, 2010