BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    CARDIMAX MODEL FX-2111

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERTEX® Reconstruction System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074239224·BONE SCREW 6955416 4.0 X 16MM CORTICAL

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981096762·Rasp, 32mm x 25mm x 16mm, 8 Deg

    FYMCO FLYER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VESSEL DILATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 12, 2014

    NFLEX STRAIG 1SEGM L150 2U PCU/TAV-ELI

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NQP·February 11, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 10, 2011