BEUDAMED
    39 results · 28ms · Sources: EU EUDAMED, US FDA

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    Tensyn Plug

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304238879·

    HHM

    FDA UDI
    Oticon A/S·05707131286970·H110V2, RITE 312 WL TC HHM

    JACOBSON GEMINI MIXTER FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896097025·JACOBSON GEMINI MIXTER FORCEPS

    DARCO HEADED CANNULATED SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ULTRA MIRAGE II MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 15, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·June 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 16, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·January 26, 2018

    SENSOR ENLITE

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·October 7, 2014

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 31, 2013

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 6, 2011

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 6, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 3, 2018