BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    TENS CONDUCTIVE MEDIA PAD

    FDA 510(k)
    FDA Class 2 ·Neurology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209123483·

    Endoform Reconstructive Template

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Holmium Laser Therapeutic Apparatus (HZ-40)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PALACOS R+G

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code LOD·April 3, 2014

    UNICEL® DXC 800 SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·December 3, 2012

    SINGLE TRIGGER ROTARY

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·September 29, 2010