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

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    BRADBURY INTRAOCULAR RETINAL KIT CAT #200

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Snowden-Pencer

    FDA UDI
    CAREFUSION 2200, INC·10885403151385·ENDOPLASTIC FIBEROPTIC ADAPTER STORZ/OLYMPUS/ACMI

    Spectra Optia Apheresis System

    FDA 510(k)
    FDA Unclassified ·Unknown

    FLEXCATH STEERABLE SHEATH & DILATOR, MODELS 3FC10, 3FC12

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POSEY KEEPSAFE DELUXE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·April 8, 2014

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·October 19, 2010

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·November 9, 2012