BEUDAMED
    7 results · 28ms · 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 ×

    MAYFIELD RADIOLUCENT 2000 SKULL CLAMP

    FDA 510(k)
    FDA Class 2 ·Neurology

    STACLOT PROTEIN S

    FDA Adverse Event
    Malfunction ·DIAGNOSTICA STAGO·Product code JGR·December 12, 1995

    DuraLazeTM HoLEP Laser Fiber

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BOSTON ES (ENFLUFOCON A), BOSTON EO (ENFLUFOCON B) AND BOSTON XO (HEXAFOCON A) RIGID GAS PERMEABLE CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 9, 2013

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·July 23, 2014

    HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·January 7, 2011