BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    ROMEO 2 PAD POSTERIOR AXIAL DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zinnanti Surgical

    FDA UDI
    Zinnanti Surgical Design Group Inc·G3731415080·6" Smoke Evac Fusion 15mm x 8mm Loop

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037534·Unitek(TM) Bicuspid Band General Purpose Narrow...

    BARCOVIEW CORONIS 5MP HD MEDICAL FLAT PANEL DISPLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT VERIO CONTROL SOLUTION

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    TOTAL ASR FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008