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

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    URETERAL DILATOR

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

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124276·Modular Offset Stem 13mm x 125mm 4mm

    300 Series Facebow

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746150654·FACEBOW LOOP STYLE 051 SIZE 4 104MM

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209108459·KIT, SURGICAL CRIC - CUSTOM

    YAHUA Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POLARIS LV, LVA APPLICATOR

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

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 5, 2014

    SPINBRUSH PRO WHITENING POWERED TOOTHBRUSH

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code JEQ·November 13, 2012

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·September 29, 2010