BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    MITEK MINI QUICKANCHOR PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MINI QA+ #0 ETH OS-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·May 9, 2018

    HALOFLEX ENERGY GENERATOR, MODELS 1190A-115A AND 1190A-230A

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

    EZ-TRAX Containment Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 4, 2013

    CAPSURE SP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014