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

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    OSTEONICS HIP REVISION WEDGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NO PROFILE

    FDA UDI
    Biomet Sports Medicine, LLC·00880304420779·

    ANATOMIC MODULAR KNEE (AMK) POSTERIOR STABILIZED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FACTOR V DEFICIENT PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·November 19, 2010

    TENDRIL DX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 1, 2014

    PUREWICK MALE EXTERNAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code NZU·September 7, 2022

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015