BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    SKYLARK MODEL 1001 TENS DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209123919·

    QT Scanner 2000 Model A

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODEL MF..D & MX..D PACEMAKER LEADS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMP,TSV,4.1MM,SBM,11.5

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·January 26, 2023

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 16, 2014

    2124215-2010-15421

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code NVZ·October 5, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 3, 2012

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 10, 2017