BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    MTS SYSTEM, WIDE-SPACE QUATTRODE PERCUTANEOUS LEADS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ArgenPMMA Multi98x30-BL

    FDA UDI
    ARGEN CORPORATION, THE·D818123299·Crown And Bridge, Temporary, Resin

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970584·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970591·

    ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROG SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADJ PIN COLLET 2.0-3.2MM

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 8, 2011

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 21, 2013

    HOMECHOICE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 26, 2014

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·February 6, 2026

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·February 6, 2026

    SmartSite Extension Set, Model No. 20029E, intravascular administration set.

    FDA Recall
    Terminated ·CareFusion 303, Inc.·Product code FPA·March 19, 2014