BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    SURGICAL IOP MONITOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717020555·OACTIVE2 CUSTOM KO L, PUSH BUTTON

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717020562·OACTIVE2 CUSTOM KO L HD, PUSH BUTTON

    ELEKTA SYNERGY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CESITRX, (LIQUID CESIUM-131 SOLUTION) FOR USE WITH GLIASITE RTS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ORTHOLOCK EX-PIN 3X110

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HAW·May 27, 2014

    LRG TAP PRI MOD NCK 8DEG 34MM

    FDA Adverse Event
    Injury ·STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI·Product code MEH·October 30, 2012

    INBONE TIBIAL BASE STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HSN·July 1, 2010