BEUDAMED
    56 results · 21ms · Sources: EU EUDAMED, US FDA

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    Tenax Laser Resistant Endotracheal Tube

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613154681624·L-PLATE, 90 DEGREE, 4MM BAR, RIGHT, STANDARD

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964085758·Trial Procedure Kit

    POWER TEK II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOPRO POLAR HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATOR LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 24, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 24, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 29, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 24, 2008

    IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 24, 2008