BEUDAMED
    11 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.

    MI-5 DIAGNOSTIC LIGHT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746086366·DB BKT LP UL CUSP 022 T=0 A+10 R=0

    ihcDirect® Calponin Ab

    FDA UDI
    NOVODIAX, INC.·00850000596030·Clone C126

    ihcDirect® Calponin Ab

    FDA UDI
    NOVODIAX, INC.·00850000596023·Clone C126

    ihcDirect® Calponin Ab Conjugate 15mL

    FDA UDI
    NOVODIAX, INC.·00850030934444·Clone C126

    ihcDirect® Calponin Ab Conjugate 5mL

    FDA UDI
    NOVODIAX, INC.·00850030934437·Clone C126

    ETI BIPOLAR HEMOSTATIC PROBE

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

    BOSCH BLOOD PRESSURE METER (BP5000 BT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 28, 2013

    WHITE RELOAD

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 17, 2010

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·July 14, 2014