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

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    GRASPING FORCEPS, RIGHT AND LEFT CURVED

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACTIVATOR V SPINAL ADJUSTING INSTRUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    PICO Single Use Negative Pressure Wound Therapy System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ASSY, PROBE, BLADDERSCAN BVI 9400/9600

    FDA Adverse Event
    Malfunction ·VERATHON INCORPORATED·Product code ITX·February 15, 2013

    TRAUMA STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·December 30, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 1, 2014

    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