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

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    LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CliP Partial Prosthesis Titanium

    FDA UDI
    Heinz Kurz GmbH·EHKM10022551·Ossicular Prosthesis, partial

    Silverbolt/Mainframe

    FDA UDI
    Choice Spine, LP·10885862161574·

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008965·PedFuse Reset, CNL, 7.0mm x 55mm

    COBE SMARXT OPTIMA XP SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEXTANT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code MCV·October 29, 2009

    COROX OTW-S 85-BP

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NKE·March 13, 2013

    ASR ACETABULAR CUPS 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    UNKNOWN DEPUY FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSA·February 20, 2008

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046603·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046696·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046429·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046160·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046320·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046795·

    NA

    FDA UDI
    Zimmer, Inc.·00889024046252·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046191·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046597·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024046641·