BEUDAMED
    7 results · 18ms · 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.
    Filters Regulation: Us FDA ×

    INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Spud

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101230·SPUD AND GOUGE REVERSIBLE HANDLE

    L582 TRANSDUCER

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

    NEUROLOGICAL SPONGE

    FDA 510(k)
    FDA Class 2 ·Neurology

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·January 22, 2013

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·December 14, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014