BEUDAMED
    7 results · 26ms · 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.

    BLADEWORKS DISPOSABLE ALK TUBING

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993591·anteriors; shade BL2; mould UBIL

    ARC 400

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    STIMPOD MODEL NMS-400 NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·March 7, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 24, 2011

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES, INC.·Product code FTM·July 28, 2014