BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    CONAIR BODY AND SOLE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SpiritMB

    FDA UDI
    ORMCO CORPORATION·00889989007381·ID U - Twin - Lower-Right Cuspid - Purple

    RESTORIS POROUS PARTIAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HES ULTRASONIC THERAPY APPLIANCE, MODELS HS-3008 (1MHZ), HS3026 (2MHZ), HS-3040 (3MHZ)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES INC.·Product code FTM·February 6, 2013

    NEURON DELIVERY CATHETER 070

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·December 14, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 22, 2014

    BD LUER-LOK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 10, 2023