BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    ORION RED URETHRAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KANAMYCIN 1000 MCG DIFFERENTIAL DISK

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ACUFIT TOTAL HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HL20 BUBBLE SENSOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015

    REM 2000 35X80 DARTEX NO FB

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code IKY·February 5, 2013

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·December 16, 2010

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2014

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 10, 2018

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·March 24, 2021