BEUDAMED
    8 results · 19ms · 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 ×

    THE C-FIT FEMORAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPEEDBAND SUPER VIEW SUPER 7

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MND·September 18, 2007

    INFINITY 252

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    AFT(R) HEP PERFORMANCE EVALUATION PROGRAM

    FDA 510(k)

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024158689·

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 15, 2013

    U0109 ACCURA SYSTEM DISP SET

    FDA Adverse Event
    Malfunction ·HAEMOTRONICS SPA·Product code KDI·January 20, 2011

    ALTRX NEUT 28IDX48OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code LPH·July 29, 2014