BEUDAMED
    6 results · 22ms · 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 ×

    PUNCTURE KIT, DISPOSALBE VEIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RELIANCE SPINAL SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zenius™, Iliad™ and Kora™ Spinal Fixation Systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE·Product code KDJ·April 30, 2014

    MERIDIAN FILTER SYSTEM - JUGULAR

    FDA Adverse Event
    Death ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·October 3, 2012

    POWER DRIVE

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code GEY·May 19, 2015