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

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    DOC VENTRAL CERVICAL STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Pristine Hemodialysis Catheter

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

    DISPOSABLE SYNTHETIC EXAMINATION GLOVES, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SUPRACONDYLAR NAIL T2 SCN 10 X 200 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code HSB·July 17, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·January 25, 2013

    MAXIMO II VR DEFIBRILLATOR

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR·Product code LWS·January 31, 2011

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014