BEUDAMED
    11 results · 17ms · Sources: EU EUDAMED, US FDA

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    PLASTILIX MINIRAD D CASSETTE

    FDA 510(k)
    FDA Class 2 ·Radiology

    ERA® Implant Abutment Micro Ang. Base, 5mm Cuff (BD)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549103919·Implant retained overdentures are an establishe...

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173005·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837189075·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837190545·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837175948·

    GENESIS REUSABLE RIGID CONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DRG DISPOSABLE VAGINAL SPECULUM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·April 17, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012

    XPERT SELF-EXPANDING TRANSHEPATIC STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR SWITZERLAND·Product code FGE·August 16, 2010