BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    GS-220 HAND IMPAIRMENT EVALUATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Malibu

    FDA UDI
    Seaspine Orthopedics Corporation·10889981081775·Tray for Rod and Cap Caddy

    BIOTEQUE SCALP VEIN SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 2, 2010

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·January 12, 2013

    ALTRUA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 3, 2014

    CIRCUIT PED 5FT DUAL-HTD 20/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BZE·June 1, 2012