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

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    ELECSYS AFP

    FDA 510(k)
    FDA Class 2 ·Immunology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981282·anteriors; shade C2; mould BIM2

    Symmetry Surgical®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482087619·Symmetry® Forceps, Tenaculum, Auto Closure Hand...

    XYLENE

    FDA 510(k)
    FDA Class 1 ·Pathology

    G3A 40 Bone Cement

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 1, 2024

    GENERATOR PULSAR2

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·February 27, 2013

    FOUNDATION SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code HSD·February 2, 2011

    7NM RATCHETING TORQUE LIMITING HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·August 5, 2014

    The Bigger Better-Bladder, Catalog Number BBB38 (with 3/8 inch ID tubing), Sterile, Single use only --- Manufactured for: Circulatory Technology Inc., 21 Singworth Street, Oyster Bay, 11771 (516) 624-2424 --- 510 (k) 981284.

    FDA Recall
    Terminated ·Circulatory Technology Inc·Product code DTN·June 3, 2009