BEUDAMED
    6 results · 23ms · 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.

    MOLIFT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Rainbow Shade

    FDA 510(k)
    FDA Class 2 ·Dental

    EQUATOR PLUS ACETABULAR CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POURCHEZ RETRO & SAFE TRAC COMBO KIT, TIP TO CUFF 23CM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD)·Product code MSD·April 11, 2014

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 4, 2010

    MEGASUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 29, 2012