BEUDAMED
    6 results · 25ms · 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.

    MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ASSAY, AMPHET. NDC#11711-0127-1 COULTER

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    EG-3670URK

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

    RX CYTOLOGY BRUSH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FDX·May 5, 2014

    CONSULTA CRT-P

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 15, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 17, 2007