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

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    OSOM STREP A TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Prestige(R) Cervical Disc System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994286970·LID 6961423 PRESTIGE SCREWS

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238065·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    SCREW-IN GUIDE TO GUIDE THREADS

    FDA Adverse Event
    Injury ·STRYKER·Product code HWC·December 28, 2017

    M2A MAGNUM 12/14 TAPER INSERTS AND ONE-PIECE MODULAR HEADS

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    DEMAND OXYGEN SAVER SYSTEM (D02S)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTAMET MTL INS NEUT 36MM 52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. REG. # 8010379·Product code KWA·February 14, 2013

    SENSIA SR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·January 14, 2011

    ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HSB·July 28, 2014