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

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    HEMOSIL VON WILLEBRAND ACTIVITY

    FDA 510(k)
    FDA Class 2 ·Hematology

    VPAP III

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO JMS APHERESIS NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·April 8, 2013

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 6, 2011

    GE OEC 2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·May 9, 2008

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018

    VITEK® 2 AST-N350

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 17, 2018

    PF-VIRTEC SYSTEM CMTED LAT.6

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·August 6, 2019