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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MAXIMA* COLLAPSIBLE VENOUS RESERVOIR BAG & HOLDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MR Wire Guide Wire Straight, MR Wire Guide Wire Angled

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 14, 2012

    HUDSON/MODIFIED TRINKLE REAMER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·September 17, 2010