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

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    AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240

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

    DURACHECK BLOOD PRESSURE CUFF, MODEL ZDC4000 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EndoTool SubQ

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARCHITECT C4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 31, 2018

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 25, 2014

    NONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·February 22, 2013

    COOL PATH DUO, 7F,1304-CP2-7-1.5(5)2-M-TE4BE1AB-CN

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - IRVINE·Product code OAD·February 3, 2011