BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Phoenix Wound Matrix

    FDA 510(k)
    FDA Unclassified ·Unknown

    IBGSTAR BLOOD GLUCOSE MONITORING SYSTEM, IBGSTAR DIABETES MANAGER APPLICATION, REV D

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PVA PLUS VIAL PVA FOAM EMBOLIZATION PARTICLES, PVA PLUS CONVENIENCE KIT PVA FOAM EMBOLIZATION PARTICLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 15, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·July 23, 2011

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 17, 2013

    UNK BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·December 8, 2017

    UNK BACTISEAL CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·December 8, 2017

    UNKNOWN VALVE/SHUNT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·November 9, 2017

    UNK EVD

    FDA Adverse Event
    Injury ·Product code JXG·January 5, 2018

    UNK EVD

    FDA Adverse Event
    Injury ·Product code JXG·January 5, 2018

    UNK EVD

    FDA Adverse Event
    Injury ·Product code JXG·January 5, 2018

    UNK EVD

    FDA Adverse Event
    Injury ·Product code JXG·January 5, 2018

    UNK EVD

    FDA Adverse Event
    Injury ·Product code JXG·January 5, 2018

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 5, 2019