BEUDAMED
    8 results · 21ms · 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.

    ECS 502

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRASOUND PROBE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FFK·July 24, 2019

    Ultrasound Probe

    FDA UDI
    BOSTON SCIENTIFIC CORPORATION·08714729516613·Ultrasound Probe

    NUNC IVF MULTIDISH 4 WELLS NUNCLON

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CLINITEK NOVUS; AUTOMATED URINE CHEMISTRY ANALYZER, 10 URINALYSIS CASSETTE, CALIBRATION KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OMNISURE MESH

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FTL·January 30, 2014

    V-PRO 1 STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code MLR·November 20, 2012

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·September 17, 2010