BEUDAMED
    6 results · 27ms · 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.

    CANNULATED PLUS HIP SCREW (STERILE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMK LANDMARK REVISION KNEE FULL WEDGE TIBIAL TRAY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NON-BALLOON REPLACEMENT GASTROSTOMY SYSTEM

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

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 11, 2013

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 24, 2014