BEUDAMED
    9 results · 39ms · Sources: EU EUDAMED, US FDA

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    Deka Luxea

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

    ICUFF REPAIR PLATE, RIGHT; CUFF REPAIR PLATE. LEFT; ANCHOR BOLT, 10MM THROUGH 50MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SEAMFREE

    FDA 510(k)
    FDA Class 2 ·Dental

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    OMNIPOD 5 POD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

    DLT TS CER HD 12/14 28MM +1.5

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) 9616671·Product code KWA·October 22, 2014

    SCD 700 COMPRESSION SYSTEM-US

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code JOW·June 19, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 30, 2011