BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    CARBON DIOXIDE - DST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707086857·BANDE ANATOMICHE SMILE I MOL LR 35

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190912·CHAMFER CUTTING BLOCK SZ 5

    MDXNET

    FDA 510(k)
    FDA Class 2 ·Radiology

    TEST, C-REATIVE PROTEIN, LATEX SLIDE

    FDA 510(k)
    FDA Class 2 ·Immunology

    COREVALVE 29MM AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 3, 2015

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·February 13, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 13, 2011

    Medtronic SOFAMOR DANEK INTREPID SPINAL SYSTEM, 5.5MM TAPERED SCREW, Length: 20MM, , Part Number: REF 7960020; 25MM, REF 7960025, 30MM, REF 7960030; and 35MM, REF 7960035; QTY: 1 EA, NON-STERILE, Rx only, MATL: TITANIUM ALLOY, Manufactured at: Warsaw, Indiana USA. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009