BEUDAMED
    94 results · 24ms · Sources: EU EUDAMED, US FDA

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    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·PROACT ADJUSTABLE CONTINENCE THERAPY FOR MEN

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·ProACT Adjustable Continence Therapy for Men

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·ProACT Adjustable Continence Therapy for Men

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·PROACT ADJUSTABLE CONTINENCE THERAPY FOR MEN

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·ProACT™ Adjustable Continence Therapy for Men

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·ProACT™ Adjustable Continence Therapy for Men

    Device, Incontinence, Mechanical/Hydraulic

    FDA Pre-Market Approval
    FDA Class 3 ·ProACT Adjustable Continence Therapy for Men

    Trestle Luxe

    FDA UDI
    ALPHATEC SPINE, INC.·00190376235974·Hexalobe Screw Removal Tool

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707009917·CALIBRA 1ST MOLAR BANDS n.UL 18

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694003025·1.6mm Rigid Curved Plate, 10 Hole

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694040877·1.6mm Rigid Curved Plate, 10 Hole, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694063951·1.6 System 10 Hole Curved Rigid Plate Sterile Q...

    Sharps Needle Destruction Device

    FDA Pre-Market Approval
    FDA Class 2 ·SHARPS TERMINATOR

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·PIPELINE EMBOLIZATION DEVICE

    NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PGQ·July 4, 2016

    NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code PGQ·August 1, 2016

    WATCHMAN ® LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NGV·February 1, 2017

    WATCHMAN ® LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NGV·July 1, 2015

    EX 45-BP, MODEL 330 132; EX 53-BP, MODEL 130 018; EX 60-BP, MODEL 330 133

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    POWERED PATIENT ROTATION BED

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code IKZ·May 24, 2013