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

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    SurgiCube

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

    SPECTRA LASER SYSTEM

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

    SOLITAIRE FR REVASCULARIZATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE S - 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 21, 2017

    DEPTH ELECTRODE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·October 10, 2014

    XIA ROD DIA. 6 X 480

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code KWQ·June 11, 2013

    AMISTEM H FEMORAL STEM CEMENTLESS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·July 6, 2011