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

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    ORATEC BIPOLAR ABLATION PROBES

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

    Monolith

    FDA UDI
    Nuvasive, Inc.·00887517676917·Monolith Core, Ø12x18mm

    Pro-Retractor Malleable Blade

    FDA UDI
    KOROS U.S.A., INC.·10840199542533·Pro-Retractor Malleable Blade Small 1-1/2 x 8"

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331131134·instrument id roll tape, withstands repeated st...

    INHALATION OPERATED NEBULIZER CODE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DBX DEMINERALIZED BONE MATRIX PUTTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code INK·March 6, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·November 30, 2016