BEUDAMED
    17 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code FSA·August 6, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FNG·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·July 25, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·July 23, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code FNG·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FNG·July 29, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code FNG·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FNG·July 22, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FNG·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FNG·July 24, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·July 31, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·August 12, 2013

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·KENSTONE METAL·Product code ITJ·April 2, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code FNG·August 2, 2013

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 18, 2019

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·July 12, 2012