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

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    RADIUS PTCA GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970466·anteriors; shade BL1; mould CS

    REVOLIX DUO LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Automatic Blood Pressure Monitor Model LD-518 & LD-537

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 29, 2017

    ADAPTA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 20, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·January 20, 2011

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 31, 2014