BEUDAMED
    6 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.

    IMPULSE EPIDURAL ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASAHI NEW PAN-SERIES HEMOFILTERS

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

    NEUROFAX 7310 SERIES (EEG)

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 19, 2014

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·December 24, 2012

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·October 25, 2010