BEUDAMED
    7 results · 20ms · 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 ×

    REPICCI II UNICONDYLAR KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KYPHON Xpede Bone Cement, CD HORIZON Fenestrated Screw Set

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MONACO RTP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNVISC ONE (HYLAN G-F 20) INJECTION

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·February 19, 2013

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code MMI·January 27, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014

    REMINGTON MEDICAL DISPOSABLE PACING CABLE

    FDA Adverse Event
    Malfunction ·REMINGTON MEDICAL·Product code DSA·September 13, 2002