BEUDAMED
    6 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 ×

    VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENTS

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

    CAMBRIDGE HEART OEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURFLO WINGED INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 24, 2013

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 20, 2011

    HS HAND CONTROLLED CURVED SHEA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·September 12, 2008