BEUDAMED
    7 results · 19ms · 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.

    MULTIPLE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209117871·

    ARTHROCARE 8000S COBLATOR SURGERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Perifix and Contiplex Catheter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·November 30, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 23, 2014

    XMTR MMT-7703NA MINILINK GST1 17L REPL

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·September 29, 2010