BEUDAMED
    7 results · 16ms · Sources: EU EUDAMED, US FDA

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    ULTRASHAPER KERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Boomerang™ Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURGICAL PROBE

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    MICRO SAGITTAL SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·March 5, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 7, 2014

    ULTRAFLEX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code ESW·February 15, 2011

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009