BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    ACL ELITE; ACL ELITE PRO

    FDA 510(k)
    FDA Class 2 ·Hematology

    REMEL

    FDA UDI
    REMEL, INC.·00848838005800·Andrades Broth w/1% Salicin 20/PK

    EQUINOX OCCULSION BALLOON SYSTEM MODEL # 104-4015, 104-4018, 104-4021, 104-4023, 104-4026

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    METRISCAN BONE DENSITY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROSPACE PEEK IMPLANT 5 7X8X22MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code MAX·June 21, 2013

    TSPACE PEEK IMPLANT 26X11X7MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code MAX·October 30, 2015

    MEDTRONIC VIRTUOSO II

    FDA Adverse Event
    MEDTRONIC·Product code LWS·April 10, 2013

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·June 11, 2008

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 15, 2011