BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    ALLFIM IMPLANT SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO HP M2376A DEVICE LINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTERLOK / HA COPELAND RESURFACING HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·February 16, 2012

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 14, 2013

    ACUITY CENTRAL MONITORING

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·March 14, 2011

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008