BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    SeaSpine Daytona Small Stature Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515023574·Volkman Retractor, USA, 4 prong, blunt, 8 3/4"

    CONMED MACROLYTE DISPERSIVE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    WESTCON HORIZON 49% (HIOXIFILCON B)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014

    ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·June 20, 2013

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·July 7, 2011

    POLYETHYLENE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQO·April 5, 2022