BEUDAMED
    18 results · 28ms · Sources: EU EUDAMED, US FDA

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    Precept

    FDA UDI
    Nuvasive, Inc.·00887517645821·PRECEPT Tap, 10.0mm Dbl Lead Cann Long

    HARPER

    FDA Adverse Event
    WATERBIRTH INTERNATIONAL·Product code ILJ·April 28, 2004

    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

    NON AC-POWERED PATIENT LIFT

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

    ARTERIAL CATHETER KIT

    FDA Adverse Event
    Injury ·ARGON MEDICAL DEVICES INC.·Product code GDY·February 19, 2019

    WALLFLEX BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 18, 2019