BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    VENTILATION MECHANICS MONITOR MODEL VMM-100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SeaSpine® Spacer System - Redondo

    FDA UDI
    Seaspine Orthopedics Corporation·10889981091484·Rasp, 15 in x 16mm

    MEGA PLUS SUPER LAG SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPLICA(TM) TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code UNK·January 30, 2013

    COLLEAGUE 3 TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP CE FRENC

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 22, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 15, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 22, 2023

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 12, 2019