BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    ARTOS, DIPLOS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970284·anteriors; shade C1; mould UBL

    Great Basin Bordetella Direct Test

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FRALEX SR 1500 LASER SYSTEM (FRALEX II SR LASER SYSTEM)

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

    DEVILBISS

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 29, 2014

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·February 20, 2013

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·January 14, 2011