BEUDAMED
    7 results · 36ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    VitalStream ART Connect; VitalStream-Hemo

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAKO Device

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLATE MUELLER HINTON II AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 26, 2022

    ALUMINA HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 4, 2008

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 9, 2011

    1.85MM TI MATRIX SCREW SELF-DRILLING/5MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JEY·July 29, 2013