BEUDAMED
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    DuraGen Secure Dural Regeneration Matrix

    FDA 510(k)
    FDA Class 2 ·Neurology

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613084875·K-Wire, Double Ended, Trocar Point, Diameter 0....

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221046390·Unitek(TM) Molar Band General Purpose Wide Hard...

    SRT100 SUPERFICIAL RADIATION THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    THE SENSITITRE AIM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE S

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 9, 2019

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·August 12, 2025

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·October 10, 2014

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 11, 2013

    ANEURX STENT GRAFT WITH XCELERANT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·June 23, 2011