BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SOFT LENS REMOVER/INSERTER/MANIPULATOR

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    CRAWFORD PORTAVAC

    FDA 510(k)

    RELIEVE LAMINOPLASTY FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEXGEN TAPER STEM PLUG

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 5, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 3, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·May 15, 2015