BEUDAMED
    65 results · 20ms · Sources: EU EUDAMED, US FDA

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    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH(TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH(TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH(TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH(TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH(TM) LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·ECONOLITH LITHOTRIPTER

    Acetabular reamer ø43mm

    FDA UDI
    Incipio Devices SA·07630055302694·Acetabular reamer for hip arthroplasty

    RESORBABLE BONE SCREW

    FDA UDI
    Biomet Orthopedics, LLC·00880304416239·

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·QVCAD SYSTEM

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS (FISH) DEVICE 5,6, AND 8 FRENCH

    JPI AUTOMATIC X-RAY FILM PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·QVCAD System (Version 3.3)

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS (FISH) DEVICE 5,6, AND 8 FRENCH

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·Femoral Introducer Sheath and Hemostasis(FISH) Device

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH & HEMOSTASIS (FISH) DEVICE

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH AND HEMOSTASIS DEVICE

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·FEMORAL INTRODUCER SHEATH & HEMOSTASIS DEVICE (FISH)

    Device, Hemostasis, Vascular

    FDA Pre-Market Approval
    FDA Class 3 ·7F FISH-SP DEVICE

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

    ACTIVA RC

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 8, 2013