BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    OR TOWEL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ELECTRODE CATHETER, ORTHOGONAL TYPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Device 300397 Putty

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RECAP SHELL COCR PC 54/48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 4, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 5, 2014

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·December 22, 2010