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

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    THREE LEVEL CONTROL SERA

    FDA 510(k)
    FDA Class 2 ·Immunology

    SUREFIRE INFUSION CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERASENSE for Zimmer Biomet Persona

    FDA 510(k)
    FDA Class 2 ·Neurology

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 15, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTE·October 31, 2012

    DORO (R) QR 3 SKULL CLAMP

    FDA Adverse Event
    Injury ·PROMED INSTRUMENTS GMBH·Product code HBL·June 1, 2015

    MICRUSFRAME10 4MM X 11.5CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 15, 2021