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

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    BARD ENDO LINK INTRACONDYLAR ROTATING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Perifit

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    INFILL GRAFT DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 20, 2014

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·August 31, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015