BEUDAMED
    16 results · 32ms · Sources: EU EUDAMED, US FDA

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    Raycell MK1

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    SUPERNOVA C5 MRI SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·July 27, 2011

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Death ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 21, 2013

    MTOME ST HOLSTER/CABLES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code KNW·September 30, 2008

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·March 17, 2022

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·September 29, 2021

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·June 3, 2022

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·August 15, 2022

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·January 30, 2023

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·February 6, 2023

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·July 27, 2021

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·November 4, 2022

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code MMX·March 28, 2022

    GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·August 18, 2022