BEUDAMED
    8 results · 17ms · 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.

    DRUGBOX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEVEL ONE CMF

    FDA UDI
    KLS-Martin L.P.·00888118094018·PLATE, MIDFACE, L SHP, W/TAB, UNI, 1.5 MM SCREW...

    SYSTEMATE CALCIUM (EPOS APPLICATION) #65409

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    THREE WHEEL SCOOTER

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HUDSON ET TUBE, UNCUFFED, 2.5

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·June 12, 2014

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·February 11, 2013

    QUICK FLEX LV LEAD

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

    Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·July 10, 2024