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.
    Filters Regulation: Us FDA ×

    APR AND APR II PRESS-FIT UNIVERSAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sterngold Implant System Guided Drill 4.75mm x 12mm.

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118852·Used to generate the bore into the bone into wh...

    WORKING CHANNEL VALVE

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    AVI MODEL 880 DUAL CHANNEL INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BELMONT RAPID INFUSER TUBING

    FDA Adverse Event
    Other ·BELMONT INSTRUMENT CORP·Product code FRN·June 26, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    TAXUS (R) LIBERTÉ (R)

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·November 23, 2010