BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    mont blanc & mont blanc MIS Spinal Systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 4

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code DQX·November 5, 2010

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2014

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·December 31, 2012