BEUDAMED
    9 results · 21ms · 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.

    E-READER

    FDA 510(k)
    FDA Class 2 ·Neurology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970436·anteriors; shade D4; mould CM

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756023696·Stockinette

    EXERCISER, EXTENSOR WAND

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    BIOMARC GOLD TISSUE MARKER

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

    BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVY·August 5, 2015

    EXPRESS¿ VASCULAR SD

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code FGE·February 20, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·July 31, 2014