BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    ULTRA BAKER JEJUNOSTOMY TUBE

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

    Precept

    FDA UDI
    Nuvasive, Inc.·00887517370143·PRECEPT Rod, 35mm

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377020741·RELINE-C Ti Rod, 3.5x35mm Straight

    HOFFRICHTER TREND 110 CPAP DEVICE WITH AQUATREND III CPAP HUMIDIFIER ACCESSORY FOR TREND

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PMT Posterior Cervical Stabilization System (PCSS)

    FDA 510(k)
    FDA Unclassified ·Unknown

    BIOPLANT

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code LYC·August 3, 2009

    BIOPLANT

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code LYC·August 3, 2009

    BIOPLANT

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code LYC·August 3, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·May 14, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·November 20, 2012

    PATIENT ROOM WALL SAVER RECL

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code FRK·September 10, 2010