BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    CELL SWEEP

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

    Khelix Steerable Electrophysiology Catheters, Khelix Loop Fixed Electrophysiology Catheters, Khelix Fixed Loop Steerable Electrophysiology Catheters, Khelix Variable Loop Steerable Electrophysiology Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DB1 EMBRYO FREEZE

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

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013

    AED 20

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code MKJ·November 22, 2010

    DEPUY ASR XL FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 3, 2014

    SMR GLENOID PEG TT SMALL-R #XL

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code KWS·December 2, 2019