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 ×

    RMI AORTIC ROOT/CORONARY SINUS MONIT./INFUSION SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V. Mueller

    FDA UDI
    CAREFUSION 2200, INC·10885403156069·DIAMOND-LINE® GRASPER INSULATED COOLEY 26CM (10...

    PLASTIC TEMPORARY ABUTMENTS, MODELS: PT341S, PT344S, PT341A, PT344A, PT451S, PT454S, PT451A, PT454A, PT561S, PT564S

    FDA 510(k)
    FDA Class 2 ·Dental

    Ethos Treatment Management, Ethos Treatment Planning, Ethos Radiotherapy System, Halcyon

    FDA 510(k)
    FDA Class 2 ·Radiology

    PULSE GEN MODEL 105

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 24, 2014

    SOLETRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·November 3, 2010

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 27, 2012