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

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    Filters Regulation: Us FDA ×

    DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-Pak

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TEPHAFLEX COMPOSITE MESH

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

    ASTRA TECH IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 13, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·September 15, 2008

    MEDISLIM

    FDA Adverse Event
    Injury ·MEDICREATIONS, LLC·Product code GEX·April 27, 2020

    PROXIMATE*75MM LINEAR CUTTER

    FDA Adverse Event
    Death ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 8, 2020

    ECHELON 45 (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Death ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 8, 2020