BEUDAMED
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    MANUAL SURGICAL INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150775·K-WIRE - SINGLE TROCAR 2.0mm DIA x 230mm

    STALIF CTI, STALIF C

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OSS/(SCARF)- AND OSW-SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·November 11, 2010

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 17, 2014

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HRX·December 27, 2012

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 16, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 16, 2024