BEUDAMED
    6 results · 24ms · 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.

    MICROSURGICAL KNIFE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SURSHIELD SAFETY WINGED INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TREZ_HD

    FDA 510(k)
    FDA Class 2 ·Neurology

    COULTER ACT DIFF 12 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 23, 2014

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·November 14, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·September 10, 2010