BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    PENCIL POINT SPINAL NEEDLE AND TRAY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CAREMIBRAIN

    FDA 510(k)
    FDA Class 2 ·Radiology

    SHORT INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 2, 2014

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·January 23, 2013

    CYCLER 220 VOLT HOMECHOICE PROAUTOMATED PD

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 18, 2010

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI, INC.·Product code EGS·May 12, 2015

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·October 9, 2025

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·December 19, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·March 1, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·June 6, 2018

    DA-800C5L

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·May 2, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018