BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    ARTHREX BIO-COMPOSITE SUTURETAK ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450325063·

    MODIFICATION TO CENTAUR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MERITS HEALTH PRODUCTS OXYGEN CONCENTRATORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 20, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 20, 2015

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·October 24, 2013

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·January 24, 2013

    GAS MODULE II

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code BZK·April 30, 2013

    RUNWAY GUIDE CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·May 17, 2011

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·July 31, 2008

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 7, 2014