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

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    MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Emprint Ablation System with Thermosphere Technology, Emprint SX Ablation Platform with Thermosphere Technology

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

    OPTISEAL ENPATH VALVED PTFE PEELABLE INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADMIRAL XTREME OTW

    FDA Adverse Event
    Malfunction ·INVATEC SPA·Product code LIT·June 25, 2014

    4.5MM CURVED BROAD LCP(TM) PL 18 HOLES/336MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·January 2, 2013

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·November 1, 2010

    WALLSTENT? RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025