BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    MULTILAB 2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    ORA Implant Abutment 3.0mm Cuff (X)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549111297·The ORA System is indicated for use with dental...

    Posicast® Thermoplastic

    FDA UDI
    MEDTEC, INC.·10841439101602·PL4392 Multiperfo sheet

    CENTERING PLUG

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

    BP50 BLOOD PRESSURE AND PULSE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TORNIER AEQUALIS REVERSE SHOLDER PROSTHESIS

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code HSD·June 18, 2009

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 1, 2014

    APEX HP ADULT HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DTZ·November 30, 2012

    MAMMOTOME EX HOLSTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·January 30, 2008