BEUDAMED
    8 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    CROSSLEAD 0.014inch

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JMS SYSLOC A.V.FISTULA NEEDLE SET

    FDA UDI
    JMS SINGAPORE PTE LTD·08888483005437·SYSLOC AVF 17GX11/4" BE 30CM W/CLAMP

    EZ-PAK (EZ-PAK IS A TRADEMARK OF IBT S.A.)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CompuFlo Epidural Computer Controlled Anesthesia System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EQUINOXE REVERSE SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 9, 2023

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    VALVE CONDUIT CONTEGRA

    FDA Adverse Event
    Death ·HEART VALVES SANTA ANA·Product code MWH·November 10, 2014

    INTRACLUDE AORTIC DEVICE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXC·July 22, 2013