BEUDAMED
    6 results · 18ms · 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 ×

    MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SMITH & NEPHEW MODEL 660HD IMAGE MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COLON-X

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

    DEVICE 8252200 NIM-RESPONSE 2.0 INTERFAC

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code ETN·February 14, 2013

    ARIA RADIATION ONCOLOGY

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS·Product code IYE·December 17, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 28, 2014