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

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    PHENYTOIN FPIA REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Tomcat Cervical Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MONITOR, AERATION, TEC-TEST

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·May 18, 2012

    HOMECHOICE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 13, 2014

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 15, 2010

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 12, 2012

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 28, 2015

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 8, 2014

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 13, 2014