BEUDAMED
    6 results · 26ms · 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 ×

    STSTORZ DP5300 AND DP9502 STERILE DRAPES

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

    MEDI-TRACE QUIKSET DX DIAG. ELECT-

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OMIBAND

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·November 24, 2010

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·January 11, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014