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

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    ALPHA MX (20)/ULTRA PC (30)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970163·anteriors; shade B1; mould ITS

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025

    SWABBABLE CAP, MODEL 60205

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Erisma® LP Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUMBER INTERBODY FUSION SYSTEM INSTRUMENTATION

    FDA Adverse Event
    Injury ·CENTERPULSE SPINE-TECH·Product code LXH·December 11, 2003

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·April 29, 2014

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 20, 2013

    QUADRA H FEMORAL STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·January 14, 2011