BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    WALLACH LEAP 100 ELECTRO SURGERY SYSTEM

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

    ZOU ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERTE-STACK SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MECTALIF POSTERIOR (TI PEEK) INTERBODY FUSION DEVICE PEEK/TI

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·June 12, 2020

    4.5MM CANNULATED SCREW FULLY THREADED/26MM

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HWC·January 18, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·December 13, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 9, 2014

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 10, 2019