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

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    DERMA SEAL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124573·Modular Offset Stem 17mm x 100mm x 2mm

    ENT BIOTECH SOLUTIONS TISSUE REMOVAL DEVICE (ELASSO)

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

    MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY

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

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 9, 2013

    DELTA

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL SYSTEMS, INC.·Product code MHX·January 4, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2014