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

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    NEUTRAL DUFFERED FORMA-SCENT

    FDA 510(k)
    FDA Class 1 ·Pathology

    ERA® Implant Abutment Micro 0°, 6mm Cuff (X)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549104893·Implant retained overdentures are an establishe...

    HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROEEG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    HEARTSTART XL+DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVY·October 31, 2012

    PD CYCLER 110 VOLT HOMECHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·August 24, 2010

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·December 8, 2017

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 8, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·December 8, 2017