BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    OCULAR CEREBRAL VASCULAR MONITOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Lacrimal Dilator

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108659·WILDER LACRIMAL DILATOR #3

    Performa®

    FDA UDI
    Merit Medical Systems, Inc.·00884450006474·

    PTFE PEEL AWAY MICROINTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Resorbable Mesh Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 2, 2014

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 2, 2012

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM·Product code DZE·July 22, 2010