BEUDAMED
    19 results · 37ms · Sources: EU EUDAMED, US FDA

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    CXI TriForce Peripheral Crossing Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRIFORCE¿ PERIPHERAL CROSSING SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·February 4, 2020

    TRIFORCE¿ PERIPHERAL CROSSING SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·January 2, 2020

    TRIFORCE¿ PERIPHERAL CROSSING SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·February 4, 2020

    TRIFORCE¿ PERIPHERAL CROSSING SET

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·January 2, 2020

    MODEL PMT850

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MYLABTWICE, MODEL 6200

    FDA 510(k)
    FDA Class 2 ·Radiology

    INFINION CX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 29, 2024

    HEARTSTART 4000

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 6, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 21, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2014

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    NESTER PLATINUM EMBOLIZATION MICROCOIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    STAINLESS STEEL EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·August 24, 2017

    Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971

    FDA Enforcement
    Class II ·Terminated·ArthroCare Corporation·September 30, 2020