BEUDAMED
    22 results · 27ms · Sources: EU EUDAMED, US FDA

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    MReye Flipper Detachable Embolization Coil and Delivery System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·April 28, 2021

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·September 12, 2018

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·September 14, 2018

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·September 14, 2018

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·April 23, 2021

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·June 14, 2021

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·April 26, 2021

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·June 13, 2019

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·September 12, 2018

    FLIPPER MREYE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·September 12, 2019

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code KRD·October 11, 2022

    AGXO

    FDA UDI
    Oticon A/S·05707131283238·H110V2, MINIBTE 312 WL 85 SGR AGXO

    POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PV 1900 SYNCHRO 0.016 GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FATHOM GUIDEWIRE

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - FREMONT·Product code DQX·June 16, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 6, 2013

    HIP HEAD, 10/12 TAPER, 28MM, +5MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 29, 2011

    ENDOPATH XCEL BLADELESS TROCAR WITH STABILITY SLEEVE - 12 MM DIAMETER, 100 MM LE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GCJ·August 28, 2008

    FATHOM GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·February 23, 2010