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

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    ANTIMICROBIAL REMOVAL DEVICE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106130·Trial, 26 x 13mm, 8 Degree, Tapered, Straight

    ELECSYS PROLACTIN II CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MAGELLAN-2200, MODEL 1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 16, 2014

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    1644487-2008-00542

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008