BEUDAMED
    6 results · 27ms · 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.

    CUSHION FLEX(TM)

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ESCOTEK-EST 221 VACUUM UNIT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    YD STRIP GPH U21

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DELTA SHUNT KIT, REGULAR, PL 1.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·May 15, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·October 27, 2010

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 22, 2012