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

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    Comet II Pressure Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHIMAERA Hip Fracture System

    FDA UDI
    ORTHOFIX SRL·18056099649292·HJ QUICK CONNECT T HANDLE

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·December 19, 2001

    NAVIX ACCESS DEVICE

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

    IDENTIUM HEAVY, IDENTIUM MEDIUM, IDENTIUM SCAN HEAVY, IDENTIUM SCAN MEDIUM, IDENTIUM SCAN LIGHT

    FDA 510(k)
    FDA Class 2 ·Dental

    SENTINOL SELF-EXPANDING NITINOL BILIARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FGE·October 7, 2008

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    KIMVENT MICROCUFF ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK HEALTH CARE·Product code BTR·August 5, 2011